A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991671



Internal ID20558711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44851597..44852080hg38UCSC Ensembl
chr11:44873148..44873631hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463339
Supporting Variants
Samples
Known GenesTSPAN18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991671
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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