A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832019



Internal ID22606954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175083535..175086280hg38UCSC Ensembl
chr2:175948263..175951008hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg382746
hg192746
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480689
Samples
Known GenesATF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832019
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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