A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1058827



Internal ID15912013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:49463856..49479582hg38UCSC Ensembl
Innerchr6:49431569..49447295hg19UCSC Ensembl
Innerchr6:49539528..49555254hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3815727
hg1915727
hg1815727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603090
Supporting Variants
Samples
Known GenesCENPQ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1058827
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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