A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472773



Internal ID21130326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54725216..54729271hg38UCSC Ensembl
chr12:55119000..55123055hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg384056
hg194056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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