A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465202



Internal ID21122755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:85805301..85879875hg38UCSC Ensembl
chr12:86199079..86273653hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3874575
hg1974575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177420
Samples
Known GenesNTS, RASSF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465202
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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