A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949877



Internal ID22725316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56652553..56652835hg38UCSC Ensembl
chr20:55227609..55227891hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949877
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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