A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697656



Internal ID15434308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103949035..103954641hg38UCSC Ensembl
Innerchr10:105708793..105714399hg19UCSC Ensembl
Innerchr10:105698783..105704389hg18UCSC Ensembl
Innerchr10:105698783..105704389hg17UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg385607
hg195607
hg185607
hg175607
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520864
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697656
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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