A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888612



Internal ID22663620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:163077607..163079283hg38UCSC Ensembl
chr2:163934117..163935793hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888612
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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