A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037160



Internal ID21946503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112963665..112963983hg38UCSC Ensembl
chr12:113401470..113401788hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609399
Samples
Known GenesOAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037160
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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