A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908620



Internal ID22683830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118631254..118634862hg38UCSC Ensembl
chr11:118501971..118505579hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383609
hg193609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356664
Samples
Known GenesPHLDB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908620
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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