A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833827



Internal ID22608762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85982018..85987346hg38UCSC Ensembl
chr2:86209141..86214469hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg385329
hg195329
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833827
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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