A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993856



Internal ID20560896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64581887..64592674hg38UCSC Ensembl
chr11:64349359..64360146hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3810788
hg1910788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460056
Supporting Variants
Samples
Known GenesSLC22A12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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