A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964227



Internal ID22739162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6090877..6090877hg38UCSC Ensembl
chr10:6132840..6132840hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361364
Samples
Known GenesRBM17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964227
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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