A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495267



Internal ID21152820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56525491..56525915hg38UCSC Ensembl
chr14:56992209..56992633hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495267
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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