A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485828



Internal ID21143381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121913245..121924596hg38UCSC Ensembl
chr12:122351151..122362502hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3811352
hg1911352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997815
Samples
Known GenesPSMD9, WDR66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485828
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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