A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462132



Internal ID21119685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:78910153..78928893hg38UCSC Ensembl
chr12:79303933..79322673hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3818741
hg1918741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184307
Samples
Known GenesSYT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462132
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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