A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994389



Internal ID63709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32470741..32473266hg38UCSC Ensembl
chr7:32510353..32512878hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg382526
hg192526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479915
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994389
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