A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482356



Internal ID21139909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118064835..118065593hg38UCSC Ensembl
chr12:118502640..118503398hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180567
Samples
Known GenesVSIG10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482356
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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