A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523569



Internal ID15104176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15591158..15599029hg38UCSC Ensembl
Innerchr10:15633157..15641028hg19UCSC Ensembl
Innerchr10:15673163..15681034hg18UCSC Ensembl
Innerchr10:15673163..15681034hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg387872
hg197872
hg187872
hg177872
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699351
Samples
Known GenesITGA8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523569
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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