A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528015



Internal ID15108622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:241701917..241907429hg38UCSC Ensembl
Innerchr1:241865219..242070731hg19UCSC Ensembl
Innerchr1:239931842..240137354hg18UCSC Ensembl
Innerchr1:238191260..238396772hg17UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38205513
hg19205513
hg18205513
hg17205513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704543
Samples
Known GenesEXO1, WDR64
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528015
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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