A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16996224



Internal ID64931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38253425..38353713hg38UCSC Ensembl
chr7:38293026..38393314hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38100289
hg19100289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141943
Supporting Variants
Samples
Known GenesTARP, TRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16996224
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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