A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995424



Internal ID64382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39931558..39934918hg38UCSC Ensembl
chr7:39971157..39974517hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg383361
hg193361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475002
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995424
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