A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473636



Internal ID21131189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:744801..771800hg38UCSC Ensembl
chr12:853967..880966hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3827000
hg1927000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185057
Samples
Known GenesWNK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473636
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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