A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703358



Internal ID15440010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67261875..67291571hg38UCSC Ensembl
Innerchr18:64929112..64958808hg19UCSC Ensembl
Innerchr18:63080092..63109788hg18UCSC Ensembl
Innerchr18:63080092..63109788hg17UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3829697
hg1929697
hg1829697
hg1729697
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526985
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703358
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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