A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604413



Internal ID16045136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104813086..104818243hg38UCSC Ensembl
Innerchr6:105260961..105266118hg19UCSC Ensembl
Innerchr6:105367654..105372811hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg385158
hg195158
hg185158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10893n54
Supporting Variantsnssv1071817
Samples
Known GenesHACE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604413
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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