A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662016



Internal ID21610321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77696322..77696322hg38UCSC Ensembl
chr17:75692404..75692404hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082183
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662016
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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