A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14286327



Internal ID22190558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33083209..33083468hg38UCSC Ensembl
chr19:33574115..33574374hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215539
Supporting Variants
SamplesHG00731
Known GenesGPATCH1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14286327
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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