A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1058818



Internal ID15565318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:49453528..49478520hg38UCSC Ensembl
Innerchr6:49421241..49446233hg19UCSC Ensembl
Innerchr6:49529200..49554192hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3824993
hg1924993
hg1824993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603081
Supporting Variants
Samples
Known GenesCENPQ, MUT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1058818
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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