A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857115



Internal ID22632050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14608893..14611292hg38UCSC Ensembl
chr10:14650892..14653291hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv148n209
Supporting Variantsnssv17469141
Samples
Known GenesFAM107B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857115
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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