A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604913



Internal ID16392322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152571603..152605382hg38UCSC Ensembl
Innerchr6:152892738..152926517hg19UCSC Ensembl
Innerchr6:152934431..152968210hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3833780
hg1933780
hg1833780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155096
Samples1780854326_A
Known GenesSYNE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604913
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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