A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832519



Internal ID22607454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224194298..224203102hg38UCSC Ensembl
chr2:225059015..225067819hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg388805
hg198805
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832519
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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