A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019214



Internal ID18761748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167382336..167805175hg38UCSC Ensembl
Innerchr6:167795824..168205855hg19UCSC Ensembl
Innerchr6:167715814..167948704hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38422840
hg19410032
hg18232891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655443
Samples
Known GenesC6orf123, TCP10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019214
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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