A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023032



Internal ID21932375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:117873116..117873196hg38UCSC Ensembl
chr12:118310921..118311001hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605320
Samples
Known GenesKSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023032
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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