A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694369



Internal ID15431021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:58257081..58265106hg38UCSC Ensembl
Innerchr1:58722753..58730778hg19UCSC Ensembl
Innerchr1:58495341..58503366hg18UCSC Ensembl
Innerchr1:58434774..58442799hg17UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg388026
hg198026
hg188026
hg178026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516742
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694369
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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