A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516489



Internal ID15097096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68513090..68536147hg38UCSC Ensembl
Innerchr15:68805429..68828486hg19UCSC Ensembl
Innerchr15:66592483..66615540hg18UCSC Ensembl
Innerchr15:66592483..66615540hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3823058
hg1923058
hg1823058
hg1723058
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662948, nssv682488, nssv704070, nssv658971, nssv668670
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516489
Frequency
Sample Size2026
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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