A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002625



Internal ID69365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129201265..129201868hg38UCSC Ensembl
chr7:128841106..128841709hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481414
Supporting Variants
Samples
Known GenesSMO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002625
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003748


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