A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956120



Internal ID22731312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36415226..36427438hg38UCSC Ensembl
chr20:35043629..35055841hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3812213
hg1912213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390746
Samples
Known GenesDLGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956120
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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