A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994395



Internal ID20561435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83849310..83863918hg38UCSC Ensembl
chr11:83560353..83574961hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3814609
hg1914609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459304
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994395
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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