A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694587



Internal ID15084553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15606244..15757643hg38UCSC Ensembl
Innerchr10:15648243..15799642hg19UCSC Ensembl
Innerchr10:15688249..15839648hg18UCSC Ensembl
Innerchr10:15688249..15839648hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38151400
hg19151400
hg18151400
hg17151400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521815
Supporting Variants
Samples
Known GenesITGA8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694587
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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