A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089465



Internal ID21440599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1035585..1035585hg38UCSC Ensembl
chr17:938825..938825hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654907
Supporting Variants
SamplesHG00732
Known GenesABR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089465
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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