A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094662



Internal ID21403171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75453311..75453311hg38UCSC Ensembl
chr17:73449392..73449392hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650010
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094662
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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