A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994635



Internal ID20561675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86719653..86720394hg38UCSC Ensembl
chr11:86430695..86431436hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464330
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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