A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524932



Internal ID15452225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:240988790..241000624hg38UCSC Ensembl
Innerchr1:241152090..241163924hg19UCSC Ensembl
Innerchr1:239218713..239230547hg18UCSC Ensembl
Innerchr1:237478131..237489965hg17UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3811835
hg1911835
hg1811835
hg1711835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700945
Samples
Known GenesRGS7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524932
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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