A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507341



Internal ID20880630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102576555..102582371hg38UCSC Ensembl
chr14:103042892..103048708hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg385817
hg195817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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