A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639023



Internal ID21587328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88103994..88103994hg38UCSC Ensembl
chr5:87399811..87399811hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149561
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639023
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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