A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605541



Internal ID16392950
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 StatusM
Merged Variants
Supporting Variantsnssv1077418
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605541
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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