A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176628



Internal ID20743669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124848436..124854757hg38UCSC Ensembl
chr9:127610715..127617036hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386322
hg196322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449578
Supporting Variants
Samples
Known GenesWDR38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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