A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875264



Internal ID22650222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31982023..31982315hg38UCSC Ensembl
chr2:32207092..32207384hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390136
Samples
Known GenesMEMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875264
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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