A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521402



Internal ID21845761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65747041..65783469hg38UCSC Ensembl
chr2:65974175..66010603hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3836429
hg1936429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989755
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521402
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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