A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000559



Internal ID67951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103137270..103137496hg38UCSC Ensembl
chr7:102777717..102777943hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488956
Supporting Variants
Samples
Known GenesNAPEPLD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000559
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