A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14372281



Internal ID22193871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113600332..113600427hg38UCSC Ensembl
chr13:114254647..114254742hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215239
Supporting Variants
SamplesHG00731
Known GenesTFDP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14372281
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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