A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018160



Internal ID18760693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93743198..93865339hg38UCSC Ensembl
Innerchr6:94452916..94575057hg19UCSC Ensembl
Innerchr6:94509637..94631778hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38122142
hg19122142
hg18122142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6093n100
Supporting Variantsnssv3648983
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)nsv1018160
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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