A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102009



Internal ID20669049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48923002..48925718hg38UCSC Ensembl
chr3:48960435..48963151hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382717
hg192717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358810
Supporting Variants
Samples
Known GenesARIH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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