A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957913



Internal ID22733007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135551430..135551430hg38UCSC Ensembl
chr5:134887120..134887120hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957913
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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