A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259235



Internal ID20468453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92153237..92153439hg38UCSC Ensembl
chr12:92547013..92547215hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736167
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259235
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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