A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671891



Internal ID15408543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60605580..60643110hg38UCSC Ensembl
Innerchr18:58272813..58310343hg19UCSC Ensembl
Innerchr18:56423793..56461323hg18UCSC Ensembl
Innerchr18:56423793..56461323hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3837531
hg1937531
hg1837531
hg1737531
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520502
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671891
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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