A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633239



Internal ID21581544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139630794..139630794hg38UCSC Ensembl
chr5:139010379..139010379hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127338
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633239
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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