A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993401



Internal ID20560442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56944127..56946789hg38UCSC Ensembl
chr11:56711602..56714264hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382663
hg192663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474502
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993401
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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