A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv455n206



Internal ID22755759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38253425..38358508hg38UCSC Ensembl
chr7:38293026..38398109hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38105084
hg19105084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6141943, nsv5485568
Samples
Known GenesTARP, TRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv455n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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