A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028367



Internal ID21937710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53313364..53313498hg38UCSC Ensembl
chr12:53707148..53707282hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600885
Samples
Known GenesAAAS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028367
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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