A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352923



Internal ID22208544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99625152..99625152hg38UCSC Ensembl
chr10:101384909..101384909hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559394
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352923
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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