A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358741



Internal ID22303215
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210342
Supporting Variants
SamplesNA19240
Known GenesTINAGL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358741
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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