A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6647n223



Internal ID22809615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38252701..38362800hg38UCSC Ensembl
chr7:38292302..38402401hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38110100
hg19110100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6605677, nsv6605567, nsv6608338
Samples
Known GenesTARP, TRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6647n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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