A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030007



Internal ID21939350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55648602..55648715hg38UCSC Ensembl
chr12:56042386..56042499hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605606
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030007
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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