A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477234



Internal ID21134787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45259058..45264804hg38UCSC Ensembl
chr14:45728261..45734007hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg385747
hg195747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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