A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574363



Internal ID16361772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:11504584..11508884hg38UCSC Ensembl
Innerchr17:11407901..11412201hg19UCSC Ensembl
Innerchr17:11348626..11352926hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384301
hg194301
hg184301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866784
Samples
Known GenesSHISA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574363
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