A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521911



Internal ID15449204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:194386445..194467211hg38UCSC Ensembl
Innerchr1:194355575..194436341hg19UCSC Ensembl
Innerchr1:192622198..192702964hg18UCSC Ensembl
Innerchr1:191087232..191167998hg17UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3880767
hg1980767
hg1880767
hg1780767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694682
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521911
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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