A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv907511



Internal ID6269438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1487771..1660801hg19UCSC Ensembl
Outerchr17:1484322..1673276hg19UCSC Ensembl
Innerchr17:1434521..1607551hg18UCSC Ensembl
Outerchr17:1431072..1620026hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1532495
SamplesMS10769
Known GenesMIR22, MIR22HG, PRPF8, RILP, SCARF1, SERPINF1, SERPINF2, SLC43A2, TLCD2, WDR81
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv907511
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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