A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495104



Internal ID272227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76761860..76761925hg38UCSC Ensembl
chr14:77228203..77228268hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697976
Samples
Known GenesVASH1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495104
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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