A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070369



Internal ID21456152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33059323..33059323hg38UCSC Ensembl
chr10:33348251..33348251hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641452
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070369
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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