A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1058666



Internal ID15911852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:48964322..49201701hg38UCSC Ensembl
Innerchr6:48931959..49169337hg19UCSC Ensembl
Innerchr6:49039918..49277296hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38237380
hg19237379
hg18237379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603049
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1058666
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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