A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832995



Internal ID22607930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:40526061..40528784hg38UCSC Ensembl
chr2:40753201..40755924hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg382724
hg192724
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485421, nssv17485420, nssv17485422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832995
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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