A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14291528



Internal ID22324442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45594721..45594856hg38UCSC Ensembl
chr19:46097979..46098114hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3535842
Supporting Variants
SamplesNA19240
Known GenesGPR4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14291528
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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