A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918176



Internal ID22693397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85344899..85349942hg38UCSC Ensembl
chr11:85055943..85060986hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385044
hg195044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362652
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918176
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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