A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021481



Internal ID20588521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82648459..82649067hg38UCSC Ensembl
chr14:83114803..83115411hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478642
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021481
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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