A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524808



Internal ID15105415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15591158..15670446hg38UCSC Ensembl
Innerchr10:15633157..15712445hg19UCSC Ensembl
Innerchr10:15673163..15752451hg18UCSC Ensembl
Innerchr10:15673163..15752451hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3879289
hg1979289
hg1879289
hg1779289
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700800
Samples
Known GenesITGA8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524808
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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