A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193020



Internal ID20760061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21192943..21200619hg38UCSC Ensembl
chr14:21661102..21668778hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg387677
hg197677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487048
Supporting Variants
Samples
Known GenesLINC00641
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193020
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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