A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668632



Internal ID15405284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:34499568..34505758hg38UCSC Ensembl
Innerchr18:32079532..32085722hg19UCSC Ensembl
Innerchr18:30333530..30339720hg18UCSC Ensembl
Innerchr18:30333530..30339720hg17UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg386191
hg196191
hg186191
hg176191
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516464
Supporting Variants
Samples
Known GenesDTNA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668632
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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