A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885828



Internal ID22660814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10013245..10014558hg38UCSC Ensembl
chr1:10073303..10074616hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381314
hg191314
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362964
Samples
Known GenesRBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885828
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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