A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029735



Internal ID87523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137686154..137701893hg38UCSC Ensembl
chr9:140580606..140596345hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3815740
hg1915740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474838
Supporting Variants
Samples
Known GenesEHMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029735
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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