A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094048



Internal ID20661088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126226341..126230475hg38UCSC Ensembl
chr3:125945184..125949318hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg384135
hg194135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360145
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094048
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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