A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033157



Internal ID89795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36470292..36470342hg38UCSC Ensembl
chr10:36759220..36759270hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033157
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.050502


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