A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384583



Internal ID21042136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52634413..52636612hg38UCSC Ensembl
chr4:53500580..53502779hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117365
Samples
Known GenesUSP46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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