A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456903



Internal ID234960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163706504..163709993hg38UCSC Ensembl
chr5:163133510..163136999hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg383490
hg193490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456903
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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