A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657452



Internal ID18609047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:49463856..49502950hg38UCSC Ensembl
Innerchr6:49431569..49470663hg19UCSC Ensembl
Innerchr6:49539528..49578622hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3839095
hg1939095
hg1839095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019611
Supporting Variants
Samples
Known GenesCENPQ, GLYATL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657452
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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