A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692155



Internal ID15082121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:50134964..50140578hg38UCSC Ensembl
Innerchr3:50172397..50178011hg19UCSC Ensembl
Innerchr3:50147401..50153015hg18UCSC Ensembl
Innerchr3:50147401..50153015hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg385615
hg195615
hg185615
hg175615
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515986
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692155
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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