A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392771



Internal ID21050324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3497327..3509193hg38UCSC Ensembl
chr5:3497441..3509307hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3811867
hg1911867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129749
Samples
Known GenesLINC01019, LOC102467075
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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