A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188225



Internal ID20755265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69365024..69365502hg38UCSC Ensembl
chr9:71979940..71980418hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439233
Supporting Variants
Samples
Known GenesFAM189A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00086


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