A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141943



Internal ID341142
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 StatusM
Merged Variantsdgv455n206
Supporting Variantsnssv16996224
Samples
Known GenesTARP, TRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141943
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer