A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995909



Internal ID20562949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104400570..104402447hg38UCSC Ensembl
chr12:104794348..104796225hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381878
hg191878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456998
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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