A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027111



Internal ID85794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120793878..120793967hg38UCSC Ensembl
chr9:123556156..123556245hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480142
Supporting Variants
Samples
Known GenesLOC100288842
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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