A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016366



Internal ID18758901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38254488..38347830hg38UCSC Ensembl
Innerchr7:38294089..38387431hg19UCSC Ensembl
Innerchr7:38260614..38353956hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3893343
hg1993343
hg1893343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6327n100
Supporting Variantsnssv3643445
Samples
Known GenesTARP, TRG-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016366
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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