A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202615



Internal ID22351753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:30758493..30758959hg38UCSC Ensembl
chr4:30760115..30760581hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14313359, nssv14313360
SamplesNA19238, NA19240
Known GenesPCDH7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202615
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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