A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599948



Internal ID21791995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121025226..121033170hg38UCSC Ensembl
chr12:121463029..121470973hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg387945
hg197945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033044
Supporting Variants
Samples
Known GenesOASL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599948
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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