A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015906



Internal ID19105124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68666344..68706439hg38UCSC Ensembl
Innerchr6:69376236..69416331hg19UCSC Ensembl
Innerchr6:69432957..69473052hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3840096
hg1940096
hg1840096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658798
Samples
Known GenesBAI3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015906
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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