A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601627



Internal ID21793674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115761476..115765261hg38UCSC Ensembl
chr12:116199281..116203066hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg383786
hg193786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032463
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601627
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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