A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227487



Internal ID22369967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9949145..9949203hg38UCSC Ensembl
chr17:9852462..9852520hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14382357
SamplesNA19238
Known GenesGAS7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227487
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer