A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908259



Internal ID6270186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41216205..41251931hg19UCSC Ensembl
Outerchr17:41213996..41278116hg19UCSC Ensembl
Innerchr17:38469731..38505457hg18UCSC Ensembl
Outerchr17:38467522..38531642hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1522513, nssv1550728
SamplesMS18554, SP53196
Known GenesBRCA1, NBR2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908259
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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