A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738938



Internal ID20514909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:8018309..8018461hg38UCSC Ensembl
chr20:7998956..7999108hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288156
Samples
Known GenesTMX4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738938
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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