A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087745



Internal ID21459486
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 StatusS
Merged Variantsnsv5664342
Supporting Variants
SamplesHG02818
Known GenesAZI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087745
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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