A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075560



Internal ID15582060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162407160..162454674hg38UCSC Ensembl
Innerchr6:162828192..162875706hg19UCSC Ensembl
Innerchr6:162748182..162795696hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3847515
hg1947515
hg1847515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605162
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)nssv1075560
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