A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834992



Internal ID22609927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151745897..151758111hg38UCSC Ensembl
chr3:151463685..151475899hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3812215
hg1912215
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485696
Samples
Known GenesAADACL2, MIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834992
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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