A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526397



Internal ID21850755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8964319..8964531hg38UCSC Ensembl
chr2:9104448..9104660hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990227
Supporting Variants
Samples
Known GenesMBOAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526397
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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