A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988260



Internal ID20555300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13435191..13435511hg38UCSC Ensembl
chr11:13456738..13457058hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439779
Supporting Variants
Samples
Known GenesBTBD10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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