A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995095



Internal ID20562135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90858073..90881141hg38UCSC Ensembl
chr11:90591241..90614309hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3823069
hg1923069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465409
Supporting Variants
Samples
Known GenesDISC1FP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995095
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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