A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575937



Internal ID16016660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69308306..69331665hg38UCSC Ensembl
Innerchr17:67304447..67327806hg19UCSC Ensembl
Innerchr17:64816042..64839401hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3823360
hg1923360
hg1823360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875916
Samples
Known GenesABCA5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575937
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