A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885884



Internal ID22660870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31985822..31985889hg38UCSC Ensembl
chr2:32210891..32210958hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392844
Samples
Known GenesMEMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885884
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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