A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033006



Internal ID89706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33309414..33321472hg38UCSC Ensembl
chr10:33598342..33610400hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3812059
hg1912059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476174
Supporting Variants
Samples
Known GenesNRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033006
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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