A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898067



Internal ID22673178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136213353..136214954hg38UCSC Ensembl
chr2:136970923..136972524hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898067
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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