A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488385



Internal ID21145938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76756472..76759920hg38UCSC Ensembl
chr14:77222815..77226263hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg383449
hg193449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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