A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832890



Internal ID22607825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37440735..37614992hg38UCSC Ensembl
chr2:37667878..37842135hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38174258
hg19174258
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484802
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832890
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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