A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032107



Internal ID89106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15603904..15761140hg38UCSC Ensembl
chr10:15645903..15803139hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38157237
hg19157237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485131
Supporting Variants
Samples
Known GenesITGA8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032107
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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