A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915800



Internal ID22691018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85041486..85072257hg38UCSC Ensembl
chr11:84752530..84783301hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3830772
hg1930772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358388
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915800
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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