A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997627



Internal ID65962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66129209..66131138hg38UCSC Ensembl
chr7:65594196..65596125hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381930
hg191930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483409
Supporting Variants
Samples
Known GenesCRCP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997627
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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