A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610401



Internal ID21802448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:37257370..37257370hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610401
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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