A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949550



Internal ID22724999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36513252..36513575hg38UCSC Ensembl
chr20:35141655..35141978hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400777
Samples
Known GenesDLGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949550
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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