A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175014



Internal ID20742054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15001877..15022598hg38UCSC Ensembl
chr9:15001875..15022596hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3820722
hg1920722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435002
Supporting Variants
Samples
Known GenesLOC389705
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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