A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464307



Internal ID242188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87431869..87454009hg38UCSC Ensembl
chr4:88353021..88375161hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3822141
hg1922141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953744
Samples
Known GenesNUDT9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464307
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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