A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996741



Internal ID20563782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102068301..102071400hg38UCSC Ensembl
chr12:102462079..102465178hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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