A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463915



Internal ID241805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77748280..77749234hg38UCSC Ensembl
chr5:77044104..77045058hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38955
hg19955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968491
Samples
Known GenesTBCA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463915
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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