A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992955



Internal ID20559995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8027584..8029458hg38UCSC Ensembl
chr11:8049131..8051005hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381875
hg191875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436969
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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