A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705763



Internal ID15095729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:53141541..53152688hg38UCSC Ensembl
Innerchr3:53175557..53186704hg19UCSC Ensembl
Innerchr3:53150597..53161744hg18UCSC Ensembl
Innerchr3:53150597..53161744hg17UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3811148
hg1911148
hg1811148
hg1711148
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517233
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705763
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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