A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026848



Internal ID85617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96856747..96974317hg38UCSC Ensembl
chr9:99619029..99736599hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38117571
hg19117571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485310
Supporting Variants
Samples
Known GenesHIATL2, LOC100132781, LOC441454, NUTM2G
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026848
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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