A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863585



Internal ID22638520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17035965..17037164hg38UCSC Ensembl
chr10:17077964..17079163hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466561
Samples
Known GenesCUBN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863585
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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