A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666081



Internal ID15056047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:133691781..133693250hg38UCSC Ensembl
Innerchr3:133410625..133412094hg19UCSC Ensembl
Innerchr3:134893315..134894784hg18UCSC Ensembl
Innerchr3:134893323..134894792hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381470
hg191470
hg181470
hg171470
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516081
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666081
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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