A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485969



Internal ID21143522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65291799..65292384hg38UCSC Ensembl
chr14:65758517..65759102hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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