A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637140



Internal ID21585445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174114294..174114294hg38UCSC Ensembl
chr5:173541297..173541297hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137427
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637140
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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