A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335366



Internal ID22210202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22665606..22669897hg38UCSC Ensembl
chr10:22954535..22958826hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384292
hg194292
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218557
Supporting Variants
SamplesHG00732
Known GenesPIP4K2A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335366
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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