A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021531



Internal ID20588572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83059984..83438606hg38UCSC Ensembl
chr14:83526328..83904950hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38378623
hg19378623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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