A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023002



Internal ID83037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39690000..39900000hg38UCSC Ensembl
chr9:41835018..42045018hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38210001
hg19210001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141968
Supporting Variants
Samples
Known GenesKGFLP2, LOC643648, MGC21881
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023002
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.233219


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