A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3535842



Internal ID22405082
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14291528, nssv14291525, nssv14291526, nssv14291527, nssv14291524
SamplesHG00512, NA19239, HG00731, NA19240, HG00733
Known GenesGPR4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3535842
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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