A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495334



Internal ID21152887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41262361..41542935hg38UCSC Ensembl
chr14:41731564..42012138hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38280575
hg19280575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018636
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495334
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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