A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492219



Internal ID21149772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52070381..52080798hg38UCSC Ensembl
chr14:52537099..52547516hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3810418
hg1910418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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