A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14291077



Internal ID22183858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1612551..1612907hg38UCSC Ensembl
chr19:1612550..1612906hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220369
Supporting Variants
SamplesHG00731
Known GenesTCF3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14291077
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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