A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664342



Internal ID21612647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81219296..81219296hg38UCSC Ensembl
chr17:79193096..79193096hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3812953
hg1912953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087745
SamplesHG02818
Known GenesAZI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664342
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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