A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476124



Internal ID21133677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61465015..61469637hg38UCSC Ensembl
chr14:61931733..61936355hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg384623
hg194623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020362
Samples
Known GenesPRKCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476124
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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