A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605469



Internal ID16392878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168316995..168317790hg38UCSC Ensembl
Innerchr6:168717675..168718470hg19UCSC Ensembl
Innerchr6:168460524..168461319hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38796
hg19796
hg18796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11068n54
Supporting Variantsnssv1077315
Samples
Known GenesDACT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605469
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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