A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188735



Internal ID20755775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:84075090..84310673hg38UCSC Ensembl
chr12:84468869..84704452hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38235584
hg19235584
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456706
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188735
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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