A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629942



Internal ID21578247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38203171..38203171hg38UCSC Ensembl
chr5:38203273..38203273hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg381151
hg191151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133678
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629942
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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