A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483008



Internal ID21140561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61169502..61173473hg38UCSC Ensembl
chr14:61636220..61640191hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg383972
hg193972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020347
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483008
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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