A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604733



Internal ID16045456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:136768384..136821808hg38UCSC Ensembl
Innerchr6:137089522..137142946hg19UCSC Ensembl
Innerchr6:137131215..137184639hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3853425
hg1953425
hg1853425
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1073591
Samples
Known GenesMAP3K5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604733
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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