A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002925



Internal ID69566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99887905..99888376hg38UCSC Ensembl
chr7:99485528..99485999hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141866
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002925
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.119597


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