A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698844



Internal ID15088810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3700636..3702688hg38UCSC Ensembl
Innerchr20:3681283..3683335hg19UCSC Ensembl
Innerchr20:3629283..3631335hg18UCSC Ensembl
Innerchr20:3629283..3631335hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382053
hg192053
hg182053
hg172053
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520565
Supporting Variants
Samples
Known GenesSIGLEC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698844
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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