A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629503



Internal ID21577808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147837649..147837649hg38UCSC Ensembl
chr5:147217212..147217212hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120389
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629503
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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