A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077244



Internal ID20644284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13840749..13842117hg38UCSC Ensembl
chr2:13980874..13982242hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg381369
hg191369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341630
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077244
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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