A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748935



Internal ID20524963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34372072..34372165hg38UCSC Ensembl
chr20:32959878..32959971hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294568
Samples
Known GenesITCH
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748935
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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