A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878386



Internal ID22653351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41773202..42005105hg38UCSC Ensembl
chr2:42000342..42232245hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38231904
hg19231904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395704
Samples
Known GenesC2orf91, LOC388942
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878386
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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