A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995236



Internal ID20562276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93589120..93595496hg38UCSC Ensembl
chr11:93322286..93328662hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386377
hg196377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469026
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995236
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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