A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3554336



Internal ID18755412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33470849..33471006hg38UCSC Ensembl
Outerchr17:33470837..33471017hg38UCSC Ensembl
Innerchr17:31797867..31798024hg19UCSC Ensembl
Outerchr17:31797855..31798035hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753083
Samples
Known GenesASIC2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3554336
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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