A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016455



Internal ID18758990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38254488..38362895hg38UCSC Ensembl
Innerchr7:38294089..38402496hg19UCSC Ensembl
Innerchr7:38260614..38369021hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38108408
hg19108408
hg18108408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6327n100
Supporting Variantsnssv3643446
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)nsv1016455
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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