A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456578



Internal ID234642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142308986..142309660hg38UCSC Ensembl
chr5:141688551..141689225hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456578
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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