A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039212



Internal ID21948555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48959096..48959273hg38UCSC Ensembl
chr12:49352879..49353056hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039212
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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