A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456917



Internal ID234974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3498724..3499446hg38UCSC Ensembl
chr5:3498838..3499560hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961520
Samples
Known GenesLINC01019, LOC102467075
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456917
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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