A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656074



Internal ID15392726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:48811490..48817295hg38UCSC Ensembl
Innerchr18:46337861..46343666hg19UCSC Ensembl
Innerchr18:44591859..44597664hg18UCSC Ensembl
Innerchr18:44591859..44597664hg17UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg385806
hg195806
hg185806
hg175806
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515638
Supporting Variants
Samples
Known GenesCTIF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656074
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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