A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490886



Internal ID21148439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118382586..118383747hg38UCSC Ensembl
chr12:118820391..118821552hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381162
hg191162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997315
Samples
Known GenesSUDS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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