A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028835



Internal ID86934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128744149..128744731hg38UCSC Ensembl
chr9:131506428..131507010hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142144
Supporting Variants
Samples
Known GenesZER1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028835
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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