A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465584



Internal ID243444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74027201..74027643hg38UCSC Ensembl
chr5:73323026..73323468hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16967115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465584
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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