A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623750



Internal ID7010606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69639987..69641318hg38UCSC Ensembl
Innerchr10:69639989..69641316hg38UCSC Ensembl
Outerchr10:69639985..69641320hg38UCSC Ensembl
chr10:71399743..71401074hg19UCSC Ensembl
Innerchr10:71399745..71401072hg19UCSC Ensembl
Outerchr10:71399741..71401076hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381332
hg191332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13856330, essv13856339, essv13856338, essv13856335, essv13856336, essv13856333, essv13856341, essv13856337, essv13856331, essv13856327, essv13856328, essv13856340, essv13856326, essv13856334, essv13856332, essv13856329
SamplesHG03300, HG03190, NA20346, HG02888, NA18510, NA19374, HG02111, HG01893, NA19235, HG03352, NA19210, NA19043, HG01130, NA20351, NA19334, NA18488
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623750
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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