A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515592



Internal ID15443203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43322734..43779976hg38UCSC Ensembl
Innerchr14:43791937..44249179hg19UCSC Ensembl
Innerchr14:42861687..43318929hg18UCSC Ensembl
Innerchr14:42861687..43318929hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38457243
hg19457243
hg18457243
hg17457243
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659981, nssv685480, nssv687811, nssv658473, nssv677373, nssv664025, nssv704217, nssv670998, nssv660406, nssv689199
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515592
Frequency
Sample Size2026
Observed Gain9
Observed Loss1
Observed Complex0
Frequencyn/a


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