A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987847



Internal ID20554887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124898246..124899487hg38UCSC Ensembl
chr11:124768142..124769383hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464800
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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