A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651950



Internal ID21600255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77776492..77776492hg38UCSC Ensembl
chr17:75772574..75772574hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091970, nssv17084164
SamplesHG03125, HG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651950
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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