A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605470



Internal ID16392879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168316995..168317914hg38UCSC Ensembl
Innerchr6:168717675..168718594hg19UCSC Ensembl
Innerchr6:168460524..168461443hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38920
hg19920
hg18920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077316
Samples
Known GenesDACT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605470
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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