A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14356294



Internal ID22182108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26494168..26494635hg38UCSC Ensembl
chr1:26820659..26821126hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197384
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14356294
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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