A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461828



Internal ID21119381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:81037494..81047165hg38UCSC Ensembl
chr12:81431273..81440944hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg389672
hg199672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461828
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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