A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694107



Internal ID15084073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1070731..1071574hg38UCSC Ensembl
Innerchr10:1116671..1117514hg19UCSC Ensembl
Innerchr10:1106671..1107514hg18UCSC Ensembl
Innerchr10:1106671..1107514hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38844
hg19844
hg18844
hg17844
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521885
Supporting Variants
Samples
Known GenesWDR37
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694107
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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