A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027278



Internal ID85906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128114972..128115685hg38UCSC Ensembl
chr9:130877251..130877964hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480953
Supporting Variants
Samples
Known GenesLOC100289019
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027278
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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