A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699649



Internal ID15436301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:61643477..61652881hg38UCSC Ensembl
Innerchr10:63403235..63412639hg19UCSC Ensembl
Innerchr10:63073241..63082645hg18UCSC Ensembl
Innerchr10:63073241..63082645hg17UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg389405
hg199405
hg189405
hg179405
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523818
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699649
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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