A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639204



Internal ID21587509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24689580..24689580hg38UCSC Ensembl
chr7:24729199..24729199hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151986
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639204
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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