A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021692



Internal ID20588732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84737840..84741813hg38UCSC Ensembl
chr14:85204184..85208157hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg383974
hg193974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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