A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074986



Internal ID15928172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159664809..159666354hg38UCSC Ensembl
Innerchr6:160085841..160087386hg19UCSC Ensembl
Innerchr6:160005831..160007376hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381546
hg191546
hg181546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604981
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)nssv1074986
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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