A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639755



Internal ID21588060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1781639..1781639hg38UCSC Ensembl
chr5:1781754..1781754hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126448
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639755
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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