A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186221



Internal ID20753262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32411405..32423463hg38UCSC Ensembl
chr12:32564339..32576397hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3812059
hg1912059
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186221
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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