A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051989



Internal ID15558489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29893694..29906838hg38UCSC Ensembl
Innerchr6:29861471..29874615hg19UCSC Ensembl
Innerchr6:29969450..29982594hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3813145
hg1913145
hg1813145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601341
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)nssv1051989
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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