A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988767



Internal ID20555807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17546664..17554306hg38UCSC Ensembl
chr11:17568211..17575853hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387643
hg197643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448740
Supporting Variants
Samples
Known GenesOTOG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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