A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977794



Internal ID22752729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123734759..123734759hg38UCSC Ensembl
chr11:123605467..123605467hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365022
Samples
Known GenesZNF202
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977794
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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