A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016642



Internal ID20583682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21203636..21204510hg38UCSC Ensembl
chr14:21671795..21672669hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490085
Supporting Variants
Samples
Known GenesLINC00641
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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