A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176890



Internal ID20743930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128639341..128652751hg38UCSC Ensembl
chr9:131401620..131415030hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3813411
hg1913411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455562
Supporting Variants
Samples
Known GenesWDR34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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