A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515638



Internal ID15443249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:48807550..48817295hg38UCSC Ensembl
Innerchr18:46333921..46343666hg19UCSC Ensembl
Innerchr18:44587919..44597664hg18UCSC Ensembl
Innerchr18:44587919..44597664hg17UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg389746
hg199746
hg189746
hg179746
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675830, nssv656074, nssv666126, nssv699334, nssv664198, nssv691452
Samples
Known GenesCTIF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515638
Frequency
Sample Size2026
Observed Gain3
Observed Loss3
Observed Complex0
Frequencyn/a


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