A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995545



Internal ID20562585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95100218..95124800hg38UCSC Ensembl
chr11:94833382..94857964hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3824583
hg1924583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470508
Supporting Variants
Samples
Known GenesENDOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995545
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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