A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516081



Internal ID15096688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:133680858..133693250hg38UCSC Ensembl
Innerchr3:133399702..133412094hg19UCSC Ensembl
Innerchr3:134882392..134894784hg18UCSC Ensembl
Innerchr3:134882400..134894792hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3812393
hg1912393
hg1812393
hg1712393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693380, nssv666081
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516081
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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