A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472749



Internal ID21130302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71795379..71796793hg38UCSC Ensembl
chr12:72189159..72190573hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg381415
hg191415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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