A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019710



Internal ID20586750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49853899..49862743hg38UCSC Ensembl
chr14:50320617..50329461hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg388845
hg198845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481699
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019710
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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