A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077418



Internal ID15930604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170129294..170162243hg38UCSC Ensembl
Innerchr6:170444518..170477467hg19UCSC Ensembl
Innerchr6:170286443..170319392hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3832950
hg1932950
hg1832950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605541
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)nssv1077418
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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