A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176882



Internal ID20743922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128511854..128512213hg38UCSC Ensembl
chr9:131274133..131274492hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438133
Supporting Variants
Samples
Known GenesGLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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