A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996504



Internal ID20563544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9896601..9898500hg38UCSC Ensembl
chr11:9918148..9920047hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438492
Supporting Variants
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996504
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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