A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656746



Internal ID21605051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76062566..76062566hg38UCSC Ensembl
chr17:74058647..74058647hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096830
SamplesHG03065
Known GenesSRP68
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656746
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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