A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704580



Internal ID15094546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3957986..4171349hg38UCSC Ensembl
Innerchr3:3999670..4213033hg19UCSC Ensembl
Innerchr3:3974670..4188033hg18UCSC Ensembl
Innerchr3:3974670..4188033hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38213364
hg19213364
hg18213364
hg17213364
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528048
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704580
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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