A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992537



Internal ID20559577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66010363..66013631hg38UCSC Ensembl
chr11:65777834..65781102hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383269
hg193269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473154
Supporting Variants
Samples
Known GenesCST6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992537
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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