A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478329



Internal ID21135882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76071813..76073181hg38UCSC Ensembl
chr14:76538156..76539524hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381369
hg191369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021167
Samples
Known GenesIFT43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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