A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3542842



Internal ID22411910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56795656..56795707hg38UCSC Ensembl
chr19:57307024..57307075hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14287399, nssv14287400, nssv14287401
SamplesHG00512, HG00513, HG00514
Known GenesZIM2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3542842
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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