A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527881



Internal ID22397267
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14368136, nssv14368135
SamplesHG00732, HG00733
Known GenesFLT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527881
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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