A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836592



Internal ID22611527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47823957..47825256hg38UCSC Ensembl
chr3:47865447..47866746hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492591
Samples
Known GenesDHX30
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836592
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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