A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614877



Internal ID21806924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:37247061..37247394hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614877
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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