A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492774



Internal ID21150327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69267187..69272921hg38UCSC Ensembl
chr14:69733904..69739638hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg385735
hg195735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020588
Samples
Known GenesGALNT16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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