A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623887



Internal ID7010743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78102962..78106419hg38UCSC Ensembl
Innerchr10:78102970..78106411hg38UCSC Ensembl
Outerchr10:78102954..78106427hg38UCSC Ensembl
chr10:79862719..79866176hg19UCSC Ensembl
Innerchr10:79862727..79866168hg19UCSC Ensembl
Outerchr10:79862711..79866184hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg383458
hg193458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13866626, essv13866627
SamplesNA19669, NA19075
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623887
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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