A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735155



Internal ID20511096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5027677..5027942hg38UCSC Ensembl
chr20:5008323..5008588hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735155
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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