A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466684



Internal ID21124237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:84532510..84591382hg38UCSC Ensembl
chr12:84926289..84985161hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3858873
hg1958873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466684
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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