A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016078



Internal ID20583118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22612378..22614974hg38UCSC Ensembl
chr14:23081284..23083877hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg382597
hg192594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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