A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837154



Internal ID22612089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88657591..88666124hg38UCSC Ensembl
chr3:88706741..88715274hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg388534
hg198534
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837154
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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