A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575936



Internal ID16016659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69268198..69331665hg38UCSC Ensembl
Innerchr17:67264339..67327806hg19UCSC Ensembl
Innerchr17:64775934..64839401hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3863468
hg1963468
hg1863468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5758n54
Supporting Variantsnssv1149794
SamplesNINDS_95
Known GenesABCA5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575936
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