A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068559



Internal ID21468658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118248313..118248313hg38UCSC Ensembl
chr10:120007825..120007825hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639242
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068559
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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