A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892682



Internal ID18836816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43603445..43630820hg38UCSC Ensembl
Outerchr15:43596778..43647444hg38UCSC Ensembl
Innerchr15:43895643..43923018hg19UCSC Ensembl
Outerchr15:43888976..43939642hg19UCSC Ensembl
Innerchr15:41682935..41710310hg18UCSC Ensembl
Outerchr15:41676268..41726934hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3850667
hg1950667
hg1850667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797016, essv25800919, essv25797698, essv25800135, essv25800051, essv25799809
Samples
Known GenesCATSPER2, CKMT1B, RNU6-28P, STRC
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892682
Frequency
Sample Size3017
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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