A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604544



Internal ID16045267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:114168157..114516017hg38UCSC Ensembl
Innerchr6:114489321..114837181hg19UCSC Ensembl
Innerchr6:114596014..114943874hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38347861
hg19347861
hg18347861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154875
SamplesHGDP00872
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604544
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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