A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829468



Internal ID22604403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:228252071..228253887hg38UCSC Ensembl
chr1:228439772..228441588hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456662
Samples
Known GenesOBSCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829468
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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