A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072061



Internal ID21450240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97647775..97647775hg38UCSC Ensembl
chr10:99407532..99407532hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg382779
hg192779
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627741
Supporting Variants
SamplesHG01114
Known GenesPI4K2A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072061
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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