A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520637



Internal ID21844996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77001421..77006450hg38UCSC Ensembl
chr2:77228547..77233576hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg385030
hg195030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990036
Supporting Variants
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520637
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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