A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666126



Internal ID15402778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:48807550..48814319hg38UCSC Ensembl
Innerchr18:46333921..46340690hg19UCSC Ensembl
Innerchr18:44587919..44594688hg18UCSC Ensembl
Innerchr18:44587919..44594688hg17UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg386770
hg196770
hg186770
hg176770
Variant TypeCNV gain
Copy Number
Allele State
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)nssv666126
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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