A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605499



Internal ID16046222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168934803..169861141hg38UCSC Ensembl
Innerchr6:169334898..170261237hg19UCSC Ensembl
Innerchr6:169076823..170003162hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38926339
hg19926340
hg18926340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077351
Samples
Known GenesC6orf120, ERMARD, LINC00242, LINC00574, PHF10, TCTE3, THBS2, WDR27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605499
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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