A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934392



Internal ID22709717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3792203..4972872hg38UCSC Ensembl
chr20:3772850..4953518hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381180670
hg191180669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390470
Samples
Known GenesADRA1D, AP5S1, CDC25B, LOC728228, MAVS, MIR103A2, MIR103B2, PANK2, PRND, PRNP, PRNT, RASSF2, RNF24, SLC23A2, SMOX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934392
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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