A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682181



Internal ID15418833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:63327736..63349197hg38UCSC Ensembl
Innerchr4:64193454..64214915hg19UCSC Ensembl
Innerchr4:63876049..63897510hg18UCSC Ensembl
Innerchr4:64022220..64043681hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3821462
hg1921462
hg1821462
hg1721462
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517519
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682181
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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