A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490736



Internal ID21148289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63748591..63755000hg38UCSC Ensembl
chr14:64215309..64221718hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg386410
hg196410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020651
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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