A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605187



Internal ID16392596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163027718..163075257hg38UCSC Ensembl
Innerchr6:163448750..163496289hg19UCSC Ensembl
Innerchr6:163368740..163416279hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3847540
hg1947540
hg1847540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075582
Samples
Known GenesPACRG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605187
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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