A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879247



Internal ID22654216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32134555..32134946hg38UCSC Ensembl
chr2:32359624..32360015hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397017
Samples
Known GenesSPAST
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879247
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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