A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14332533



Internal ID22116310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13713817..13713876hg38UCSC Ensembl
chr10:13755817..13755876hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219087
Supporting Variants
SamplesHG00512
Known GenesFRMD4A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14332533
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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