A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464110



Internal ID21121663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56388294..56392272hg38UCSC Ensembl
chr12:56782078..56786056hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg383979
hg193979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464110
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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