A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906968



Internal ID22682172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186235823..186262672hg38UCSC Ensembl
chr2:187100550..187127399hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3826850
hg1926850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906968
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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