A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515615



Internal ID15443226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161687306..161845996hg38UCSC Ensembl
Innerchr3:161405094..161563784hg19UCSC Ensembl
Innerchr3:162887788..163046478hg18UCSC Ensembl
Innerchr3:162887796..163046486hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38158691
hg19158691
hg18158691
hg17158691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695607, nssv688972, nssv664110, nssv679782, nssv672159, nssv690533
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515615
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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