A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479707



Internal ID21137260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36325469..36326231hg38UCSC Ensembl
chr14:36794675..36795437hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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