A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878768



Internal ID22653733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:82917019..83002093hg38UCSC Ensembl
chr2:83144143..83229217hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3885075
hg1985075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878768
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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