A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996899



Internal ID20563939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110144344..110144993hg38UCSC Ensembl
chr12:110582149..110582798hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478795
Supporting Variants
Samples
Known GenesIFT81
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00017


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