A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189570



Internal ID20756610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3495001..3496300hg38UCSC Ensembl
chr9:3495001..3496300hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427522
Supporting Variants
Samples
Known GenesRFX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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