A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296236



Internal ID20505454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27008065..27009427hg38UCSC Ensembl
chr12:27160998..27162360hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg381363
hg191363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736808
Supporting Variants
Samples
Known GenesTM7SF3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296236
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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