A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992614



Internal ID62552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7544242..7562242hg38UCSC Ensembl
chr7:7583873..7601873hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3818001
hg1918001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466966
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992614
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