A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456637



Internal ID21114190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93991589..93994714hg38UCSC Ensembl
chr12:94385365..94388490hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg383126
hg193126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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