A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890515



Internal ID22665543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186118613..186178916hg38UCSC Ensembl
chr2:186983340..187043643hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3860304
hg1960304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890515
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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