A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482661



Internal ID21140214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52388539..52389275hg38UCSC Ensembl
chr14:52855257..52855993hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019995
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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