A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987329



Internal ID20554371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126214118..126216114hg38UCSC Ensembl
chr11:126084013..126086009hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381997
hg191997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463127
Supporting Variants
Samples
Known GenesFAM118B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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