A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832511



Internal ID22607446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220832471..220836178hg38UCSC Ensembl
chr2:221697191..221700898hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg383708
hg193708
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832511
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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