A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865618



Internal ID22640553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17080503..17103623hg38UCSC Ensembl
chr10:17122502..17145622hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3823121
hg1923121
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452150
Samples
Known GenesCUBN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865618
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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