A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577682



Internal ID21769725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18942027..18942109hg38UCSC Ensembl
chr9:18942025..18942107hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006340
Supporting Variants
Samples
Known GenesFAM154A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577682
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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