A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023499



Internal ID21932842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:117357903..117357966hg38UCSC Ensembl
chr12:117795708..117795771hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600095
Samples
Known GenesNOS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023499
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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