A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919435



Internal ID22694657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84554305..84639462hg38UCSC Ensembl
chr11:84265348..84350505hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3885158
hg1985158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364523
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919435
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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