A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605580



Internal ID16392989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170561488..170581515hg38UCSC Ensembl
Innerchr6:170870576..170890603hg19UCSC Ensembl
Innerchr6:170712501..170732528hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3820028
hg1920028
hg1820028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077585
Samples
Known GenesPDCD2, TBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605580
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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