A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14286476



Internal ID22301093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37242099..37242198hg38UCSC Ensembl
chr19:37733001..37733100hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeOTHER complex substitution
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525746
Supporting Variants
SamplesNA19240
Known GenesZNF383
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14286476
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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