A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392449



Internal ID21050002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39383263..39383719hg38UCSC Ensembl
chr5:39383365..39383821hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130786
Samples
Known GenesDAB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392449
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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