A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600508



Internal ID21792555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22869632..22869632hg38UCSC Ensembl
chr12:23022566..23022566hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091119
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600508
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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