A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv470587



Internal ID6059764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41221596..41298854hg19UCSC Ensembl
Innerchr17:38475122..38552380hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv547474
SamplesHGDP01028
Known GenesBRCA1, NBR2
Method
AnalysisOverlapping CNVs were merged. The positions are based on the farthest SNPs observed anomg any individuals with the CNV.
PlatformIllumina HumanHap550 Genotyping BeadChip v1 + v3
Comments
ReferenceJakobsson et al 2008
Pubmed ID18288195
Accession Number(s)nsv470587
Frequency
Sample Size443
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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