A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036235



Internal ID21945578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64975013..64975395hg38UCSC Ensembl
chr14:65441731..65442113hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615367
Samples
Known GenesCHURC1-FNTB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036235
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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