A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744320



Internal ID20520319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37583516..37583580hg38UCSC Ensembl
chr5:37583618..37583682hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294057
Samples
Known GenesWDR70
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744320
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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