A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701408



Internal ID15438060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129196748..129202586hg38UCSC Ensembl
Innerchr3:128915591..128921429hg19UCSC Ensembl
Innerchr3:130398281..130404119hg18UCSC Ensembl
Innerchr3:130398289..130404127hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg385839
hg195839
hg185839
hg175839
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525302
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701408
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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