A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075514



Internal ID15582014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162171775..162255532hg38UCSC Ensembl
Innerchr6:162592807..162676564hg19UCSC Ensembl
Innerchr6:162512797..162596554hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3883758
hg1983758
hg1883758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605110
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075514
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