A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3306325



Internal ID15153273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96777994..96777995hg38UCSC Ensembl
Innerchr15:96777976..96778013hg38UCSC Ensembl
Outerchr15:96777975..96778014hg38UCSC Ensembl
chr15:97321224..97321225hg19UCSC Ensembl
Innerchr15:97321206..97321243hg19UCSC Ensembl
Outerchr15:97321205..97321244hg19UCSC Ensembl
chr15:95122228..95122229hg18UCSC Ensembl
Innerchr15:95122247..95122210hg18UCSC Ensembl
Outerchr15:95122209..95122248hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38306
hg19306
hg18306
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7808628, essv7770477, essv7778216, essv7779066, essv7815642, essv7830450, essv7776764, essv7827269, essv7800184, essv7815907, essv7793478, essv7792587, essv7791570, essv7803261, essv7784800, essv7826318, essv7819568, essv7797982, essv7823772, essv7788063, essv7785735, essv7821522, essv7807762, essv7820840, essv7804794, essv7802583, essv7780888, essv7804902, essv7818595, essv7794654, essv7783205, essv7826988, essv7774767, essv7811887, essv7803666, essv7795724, essv7830329, essv7816560, essv7799205, essv7775626, essv7783420, essv7823031, essv7807615, essv7814649, essv7830969, essv7773467, essv7774290, essv7828821, essv7822288, essv7790731, essv7805233, essv7810177, essv7772765, essv7818927, essv7798622
SamplesNA12414, NA18507, NA18603, NA12045, NA18545, NA12004, NA19190, NA18526, NA12155, NA18563, NA19005, NA18944, NA12812, NA18558, NA18960, NA18942, NA18582, NA18571, NA18964, NA12156, NA12044, NA11994, NA18520, NA18973, NA18638, NA18951, NA18605, NA12003, NA18572, NA12234, NA18537, NA18566, NA18573, NA11919, NA18532, NA18853, NA18555, NA18570, NA18858, NA18593, NA18576, NA18608, NA18542, NA11881, NA19108, NA18961, NA18952, NA18564, NA18943, NA07037, NA12763, NA12749, NA18552, NA07000, NA18562
Known GenesSPATA8-AS1
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3306325
Frequency
Sample Size185
Observed Gain55
Observed Loss0
Observed Complex0
Frequencyn/a


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