A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145951



Internal ID345156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65052836..65052889hg38UCSC Ensembl
chr14:65519554..65519607hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696760
Samples
Known GenesCHURC1-FNTB, FNTB, MAX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145951
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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