A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604147



Internal ID16391556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92390188..92430198hg38UCSC Ensembl
Innerchr6:93099906..93139916hg19UCSC Ensembl
Innerchr6:93156627..93196637hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3840011
hg1940011
hg1840011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10840n54
Supporting Variantsnssv1155764
SamplesHGDP00948
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604147
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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