A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899373



Internal ID22674503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236714659..236715168hg38UCSC Ensembl
chr2:237623302..237623811hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899373
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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