A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021482



Internal ID19110700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167194096..167243961hg38UCSC Ensembl
Innerchr6:167607584..167657449hg19UCSC Ensembl
Innerchr6:167527574..167577439hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3849866
hg1949866
hg1849866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6195n100
Supporting Variantsnssv3655404
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)nsv1021482
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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