A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072108



Internal ID21482943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99405079..99405079hg38UCSC Ensembl
chr10:101164836..101164836hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644165
Supporting Variants
SamplesHG03732
Known GenesGOT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072108
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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