A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069555



Internal ID21466333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20659649..20659649hg38UCSC Ensembl
chr10:20948578..20948578hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641818
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069555
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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