A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834948



Internal ID22609883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142566750..142573121hg38UCSC Ensembl
chr3:142285592..142291963hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg386372
hg196372
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485202
Samples
Known GenesATR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834948
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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