A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994619



Internal ID20561659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86570448..86571000hg38UCSC Ensembl
chr11:86281490..86282042hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472115
Supporting Variants
Samples
Known GenesME3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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