A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220532



Internal ID22365199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35045650..35045719hg38UCSC Ensembl
chr19:35536554..35536623hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286383, nssv14286382, nssv14286384
SamplesHG00512, HG00513, HG00514
Known GenesHPN
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220532
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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