A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029697



Internal ID87500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137429849..137430143hg38UCSC Ensembl
chr9:140324301..140324595hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475082
Supporting Variants
Samples
Known GenesNOXA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029697
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.015303


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