A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268722



Internal ID20477940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97132608..97132608hg38UCSC Ensembl
chr12:97526386..97526386hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754615
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268722
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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