A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997016



Internal ID20564057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11247945..11248229hg38UCSC Ensembl
chr12:11400852..11401136hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471555
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00174


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