A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385891



Internal ID22268422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8671492..8671546hg38UCSC Ensembl
chr17:8574810..8574864hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527016
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385891
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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