A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994691



Internal ID20561731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84834665..84920251hg38UCSC Ensembl
chr11:84545708..84631295hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3885587
hg1985588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466959
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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