A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182197



Internal ID20749237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6397804..6407970hg38UCSC Ensembl
chr12:6506970..6517136hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3810167
hg1910167
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470913
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182197
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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