A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177284



Internal ID20744324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:23264652..23287974hg38UCSC Ensembl
chr12:23417586..23440908hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3823323
hg1923323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457497
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177284
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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