A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879423



Internal ID22654392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44958127..44958230hg38UCSC Ensembl
chr2:45185266..45185369hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393286
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879423
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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