A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282536



Internal ID20491754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2768346..2768346hg38UCSC Ensembl
chr12:2877512..2877512hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755811
Supporting Variants
Samples
Known GenesLOC283440
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282536
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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