A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664876



Internal ID15401528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:135716655..135739111hg38UCSC Ensembl
Innerchr3:135435497..135457953hg19UCSC Ensembl
Innerchr3:136918187..136940643hg18UCSC Ensembl
Innerchr3:136918195..136940651hg17UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3822457
hg1922457
hg1822457
hg1722457
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515820
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664876
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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