A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886185



Internal ID22661171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74096514..74096838hg38UCSC Ensembl
chr2:74323641..74323965hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401448
Samples
Known GenesTET3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886185
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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