A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575928



Internal ID16016651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68898720..68917795hg38UCSC Ensembl
Innerchr17:66894861..66913936hg19UCSC Ensembl
Innerchr17:64406456..64425531hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3819076
hg1919076
hg1819076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875909
Samples
Known GenesABCA8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575928
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