A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070352



Internal ID21467292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30611702..30611702hg38UCSC Ensembl
chr10:30900631..30900631hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639841
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070352
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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