A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600681



Internal ID21792728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45317107..45317107hg38UCSC Ensembl
chr12:45710890..45710890hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083152
Supporting Variants
Samples
Known GenesANO6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600681
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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