A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211509



Internal ID22359047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42207953..42208434hg38UCSC Ensembl
chr17:40359971..40360452hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14379487
SamplesHG00512
Known GenesSTAT5B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211509
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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