A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703900



Internal ID127566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68386874..68395500hg38UCSC Ensembl
chr15:68679213..68687839hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388627
hg198627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531939
Supporting Variants
Samples
Known GenesITGA11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703900
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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