A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884320



Internal ID22659302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20069332..20069708hg38UCSC Ensembl
chr2:20269093..20269469hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884320
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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