A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527999



Internal ID15108606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1325319..1422697hg38UCSC Ensembl
Innerchr10:1367514..1464892hg19UCSC Ensembl
Innerchr10:1357514..1454892hg18UCSC Ensembl
Innerchr10:1357514..1454892hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3897379
hg1997379
hg1897379
hg1797379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704524
Samples
Known GenesADARB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527999
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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