A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836452



Internal ID22611387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64896875..64897974hg38UCSC Ensembl
chr3:64882550..64883649hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494043
Samples
Known GenesADAMTS9-AS2, MIR548A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836452
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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