A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954837



Internal ID22730065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23524091..23524091hg38UCSC Ensembl
chr1:23850583..23850583hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361841
Samples
Known GenesE2F2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954837
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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