A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023020



Internal ID83053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61518808..61664808hg38UCSC Ensembl
chr9:44726647..44872646hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38146001
hg19146000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482996
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023020
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.999674


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