A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603765



Internal ID21795812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64589446..64590002hg38UCSC Ensembl
chr12:64983226..64983782hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38557
hg19557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603765
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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