A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487678



Internal ID21145231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65662701..65664200hg38UCSC Ensembl
chr14:66129419..66130918hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020771
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487678
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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