A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996905



Internal ID20563945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110244049..110247170hg38UCSC Ensembl
chr12:110681854..110684975hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg383122
hg193122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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