A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830902



Internal ID22605837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113769192..113773942hg38UCSC Ensembl
chr2:114526769..114531519hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg384751
hg194751
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830902
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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