A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637413



Internal ID21585718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131030126..131030126hg38UCSC Ensembl
chr5:130365819..130365819hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127174
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637413
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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