A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521682



Internal ID15448975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:203113683..203114880hg38UCSC Ensembl
Innerchr1:203082811..203084008hg19UCSC Ensembl
Innerchr1:201349434..201350631hg18UCSC Ensembl
Innerchr1:199814468..199815665hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381198
hg191198
hg181198
hg171198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698302
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521682
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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