A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624374



Internal ID7011230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101283105..101284940hg38UCSC Ensembl
Innerchr10:101283105..101284940hg38UCSC Ensembl
Outerchr10:101282782..101285348hg38UCSC Ensembl
chr10:103042862..103044697hg19UCSC Ensembl
Innerchr10:103042862..103044697hg19UCSC Ensembl
Outerchr10:103042539..103045105hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381836
hg191836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13913058, essv13913052, essv13913067, essv13913049, essv13913060, essv13913053, essv13913065, essv13913061, essv13913057, essv13913055, essv13913051, essv13913064, essv13913059, essv13913050, essv13913062, essv13913048, essv13913066, essv13913063, essv13913056, essv13913054
SamplesNA18599, HG02078, HG02384, HG02087, HG02374, HG02402, NA18573, HG00525, HG00864, HG02399, HG00611, HG00580, HG02188, HG02133, HG01801, HG01804, HG01028, HG02079, HG02113, HG01600
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624374
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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