A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192626



Internal ID22343180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150334090..150334540hg38UCSC Ensembl
chr1:150306561..150307011hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14288411, nssv14288412
SamplesHG00512, HG00732
Known GenesPRPF3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192626
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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