A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17006006



Internal ID71618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157125658..157125823hg38UCSC Ensembl
chr7:156918352..156918517hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17006006
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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