A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868212



Internal ID22643147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15840910..15840961hg38UCSC Ensembl
chr2:15981034..15981085hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868212
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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