A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030170



Internal ID87830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134078305..134081869hg38UCSC Ensembl
chr9:136943427..136946991hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg383565
hg193565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030170
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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