A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473614



Internal ID21131167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4958268..4959157hg38UCSC Ensembl
chr12:5067434..5068323hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473614
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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