A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030631



Internal ID19119850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:62401893..62515792hg38UCSC Ensembl
Innerchr6:63111798..63225697hg19UCSC Ensembl
Innerchr6:63169757..63283656hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38113900
hg19113900
hg18113900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657643
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030631
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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