A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605540



Internal ID16392949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170129294..170151634hg38UCSC Ensembl
Innerchr6:170444518..170466858hg19UCSC Ensembl
Innerchr6:170286443..170308783hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3822341
hg1922341
hg1822341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155824
SamplesHGDP00518
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605540
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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