A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033512



Internal ID90028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30024535..30024613hg38UCSC Ensembl
chr10:30313464..30313542hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477324
Supporting Variants
Samples
Known GenesKIAA1462
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033512
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