A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6327n100



Internal ID20157943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38254488..38362895hg38UCSC Ensembl
chr7:38294089..38402496hg19UCSC Ensembl
chr7:38260614..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 Variants
Supporting Variantsnsv1016366, nsv1016455
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)dgv6327n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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