A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574359



Internal ID16015082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:11223935..11275051hg38UCSC Ensembl
Innerchr17:11127252..11178368hg19UCSC Ensembl
Innerchr17:11067977..11119093hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3851117
hg1951117
hg1851117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866782
Samples
Known GenesSHISA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574359
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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