A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3306875



Internal ID15153823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127392027..127392028hg38UCSC Ensembl
Innerchr10:127392010..127392045hg38UCSC Ensembl
Outerchr10:127392009..127392046hg38UCSC Ensembl
chr10:129190291..129190292hg19UCSC Ensembl
Innerchr10:129190274..129190309hg19UCSC Ensembl
Outerchr10:129190273..129190310hg19UCSC Ensembl
chr10:129080281..129080282hg18UCSC Ensembl
Innerchr10:129080299..129080264hg18UCSC Ensembl
Outerchr10:129080263..129080300hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38291
hg19291
hg18291
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7824098, essv7797297, essv7785010, essv7791450, essv7829745, essv7817252, essv7820510, essv7830088, essv7777842, essv7816680, essv7807218, essv7793563, essv7781544, essv7835673, essv7806589, essv7823414, essv7773958, essv7829616, essv7787550, essv7801782, essv7812357, essv7804653, essv7794925, essv7789733, essv7821575, essv7817433, essv7796671, essv7822658, essv7784057, essv7815573, essv7787988, essv7796170, essv7781920, essv7811764, essv7809168, essv7824886, essv7814982, essv7802210, essv7834165, essv7782233, essv7779664, essv7782788, essv7811310, essv7798149, essv7821058, essv7828887, essv7803001, essv7827360, essv7800079, essv7835018, essv7814315
SamplesNA18502, NA19141, NA18947, NA11995, NA18592, NA11931, NA12045, NA12751, NA18526, NA07346, NA18550, NA12812, NA18558, NA18942, NA11992, NA07347, NA18949, NA12761, NA12044, NA11994, NA18973, NA18638, NA12489, NA18871, NA18948, NA12234, NA18907, NA19114, NA12249, NA18523, NA18570, NA18576, NA12043, NA18608, NA11881, NA19108, NA18517, NA12873, NA12874, NA07037, NA19143, NA18501, NA19093, NA18609, NA18552, NA12006, NA12154, NA18562, NA12776, NA18965, NA18577
Known GenesDOCK1
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3306875
Frequency
Sample Size185
Observed Gain51
Observed Loss0
Observed Complex0
Frequencyn/a


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