A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022802



Internal ID21932145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12594025..12595144hg38UCSC Ensembl
chr12:12746959..12748078hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg381120
hg191120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022802
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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