A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028637



Internal ID86792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124714496..124714630hg38UCSC Ensembl
chr9:127476775..127476909hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482824
Supporting Variants
Samples
Known GenesNR6A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028637
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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