A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029952



Internal ID18772483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164042323..164855422hg38UCSC Ensembl
Innerchr6:164463355..165268911hg19UCSC Ensembl
Innerchr6:164383345..165188901hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38813100
hg19805557
hg18805557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749615
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029952
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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