A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994620



Internal ID20561660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86572023..86584223hg38UCSC Ensembl
chr11:86283065..86295265hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3812201
hg1912201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469644
Supporting Variants
Samples
Known GenesME3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994620
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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