A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479923



Internal ID257437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66948315..66948654hg38UCSC Ensembl
chr8:67860550..67860889hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011790
Samples
Known GenesTCF24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479923
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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