A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996165



Internal ID20563205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10769550..10770389hg38UCSC Ensembl
chr12:10922149..10922988hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468867
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996165
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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