A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831701



Internal ID22606636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160074257..160076459hg38UCSC Ensembl
chr2:160930768..160932970hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg382203
hg192203
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480590
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831701
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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