A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605502



Internal ID16392911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169098207..169116101hg38UCSC Ensembl
Innerchr6:169498302..169516196hg19UCSC Ensembl
Innerchr6:169240227..169258121hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3817895
hg1917895
hg1817895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155809
SamplesHGDP00717
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605502
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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