A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072627



Internal ID21401663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99838925..99838925hg38UCSC Ensembl
chr10:101598682..101598682hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635999
Supporting Variants
SamplesHG00096
Known GenesABCC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072627
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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