A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632957



Internal ID21581262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11488..11488hg38UCSC Ensembl
chr5:11488..11488hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120393
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632957
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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