A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486542



Internal ID21144095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42665651..42666775hg38UCSC Ensembl
chr14:43134854..43135978hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg381125
hg191125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486542
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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