A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033177



Internal ID89809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36639130..37728964hg38UCSC Ensembl
chr10:36928058..38017892hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg381089835
hg191089835
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488790
Supporting Variants
Samples
Known GenesANKRD30A, LINC00993, MTRNR2L7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033177
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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