A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847751



Internal ID22622686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16945505..17014141hg38UCSC Ensembl
chr10:16987504..17056140hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3868637
hg1968637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457194, nssv17456497
Samples
Known GenesCUBN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847751
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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