A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224815



Internal ID22368134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30130714..30130807hg38UCSC Ensembl
chr19:30621621..30621714hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4234n152
Supporting Variantsnssv14285862, nssv14285860, nssv14285861
SamplesNA19238, HG00731, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224815
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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