A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035287



Internal ID91258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71912104..71912402hg38UCSC Ensembl
chr10:73671862..73672160hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478501
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035287
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.005153


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