A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995597



Internal ID20562637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95770001..95770900hg38UCSC Ensembl
chr11:95503165..95504064hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474677
Supporting Variants
Samples
Known GenesFAM76B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995597
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00079


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