A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604793



Internal ID16392202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141892956..141962061hg38UCSC Ensembl
Innerchr6:142214093..142283198hg19UCSC Ensembl
Innerchr6:142255786..142324891hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3869106
hg1969106
hg1869106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155787
SamplesHGDP00868
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604793
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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