A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895049



Internal ID22670126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224653033..224660331hg38UCSC Ensembl
chr2:225517750..225525048hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg387299
hg197299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895049
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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