A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210342



Internal ID22358278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31578440..31578606hg38UCSC Ensembl
chr1:32044041..32044207hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv176n152
Supporting Variantsnssv14358740, nssv14358741
SamplesNA19238, NA19240
Known GenesTINAGL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210342
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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