A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492062



Internal ID21149615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75974978..75979664hg38UCSC Ensembl
chr14:76441321..76446007hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384687
hg194687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021164
Samples
Known GenesTGFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer