A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094402



Internal ID20661442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143500750..143502374hg38UCSC Ensembl
chr3:143219592..143221216hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381625
hg191625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356315
Supporting Variants
Samples
Known GenesSLC9A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02552


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