A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178096



Internal ID20745136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31808248..31851639hg38UCSC Ensembl
chr12:31961182..32004573hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3843392
hg1943392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468471
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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