A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14368136



Internal ID22222295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28377409..28377475hg38UCSC Ensembl
chr13:28951546..28951612hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527881
Supporting Variants
SamplesHG00733
Known GenesFLT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14368136
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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