A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949183



Internal ID22724634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119251104..119251104hg38UCSC Ensembl
chr1:119793727..119793727hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949183
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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