A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734224



Internal ID20510159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48867637..48867693hg38UCSC Ensembl
chr20:47484174..47484230hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734224
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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