A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021069



Internal ID20588109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72852298..72856820hg38UCSC Ensembl
chr14:73319006..73323528hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg384523
hg194523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479633
Supporting Variants
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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