A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463508



Internal ID21121061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62674864..62709024hg38UCSC Ensembl
chr12:63068644..63102804hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3834161
hg1934161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002110
Samples
Known GenesPPM1H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463508
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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