A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285029



Internal ID20494247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16510972..16510972hg38UCSC Ensembl
chr12:16663906..16663906hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763448
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285029
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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