A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351412



Internal ID21008965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168778410..168785410hg38UCSC Ensembl
chr2:169634920..169641920hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg387001
hg197001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079930
Samples
Known GenesCERS6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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