A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605343



Internal ID16046066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167283902..167302555hg38UCSC Ensembl
Innerchr6:167697390..167716043hg19UCSC Ensembl
Innerchr6:167617380..167636033hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3818654
hg1918654
hg1818654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077046
Samples
Known GenesUNC93A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605343
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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