A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601673



Internal ID16389082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31314446..31352761hg38UCSC Ensembl
Innerchr6:31282223..31320538hg19UCSC Ensembl
Innerchr6:31390202..31428517hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3838316
hg1938316
hg1838316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10381n54
Supporting Variantsnssv1053035
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601673
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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