A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480374



Internal ID21137927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83509120..83509777hg38UCSC Ensembl
chr14:83975464..83976121hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480374
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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