A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019452



Internal ID18761987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93769864..93875011hg38UCSC Ensembl
Innerchr6:94479582..94584729hg19UCSC Ensembl
Innerchr6:94536303..94641450hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38105148
hg19105148
hg18105148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6093n100
Supporting Variantsnssv3751236
Samples
Known GenesTSG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019452
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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