A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669300



Internal ID15405952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59987001..60008626hg38UCSC Ensembl
Innerchr18:57654233..57675858hg19UCSC Ensembl
Innerchr18:55805213..55826838hg18UCSC Ensembl
Innerchr18:55805213..55826838hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3821626
hg1921626
hg1821626
hg1721626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515764
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669300
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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