A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154858



Internal ID15855999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104449043..104486604hg38UCSC Ensembl
Innerchr6:104896918..104934479hg19UCSC Ensembl
Innerchr6:105003611..105041172hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3837562
hg1937562
hg1837562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604393
Supporting Variants
Samples1798860306_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154858
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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