A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464024



Internal ID21121577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62384984..62412282hg38UCSC Ensembl
chr12:62778765..62806062hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3827299
hg1927298
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192112
Samples
Known GenesUSP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464024
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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