A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993470



Internal ID20560510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67141573..67157625hg38UCSC Ensembl
chr11:66909044..66925096hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3816053
hg1916053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462720
Supporting Variants
Samples
Known GenesKDM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993470
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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