A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458904



Internal ID21116457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:81903583..81904103hg38UCSC Ensembl
chr12:82297362..82297882hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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