A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623796



Internal ID7010652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72304397..72318302hg38UCSC Ensembl
Innerchr10:72304897..72317802hg38UCSC Ensembl
Outerchr10:72303397..72319302hg38UCSC Ensembl
chr10:74064155..74078060hg19UCSC Ensembl
Innerchr10:74064655..74077560hg19UCSC Ensembl
Outerchr10:74063155..74079060hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3813906
hg1913906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861597, essv13861598, essv13861596
SamplesNA19917, HG03644, HG01589
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623796
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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