A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831178



Internal ID22606113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112590475..112593954hg38UCSC Ensembl
chr2:113348052..113351531hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg383480
hg193480
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485028, nssv17485029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831178
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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