A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605156



Internal ID16045879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162354823..162467672hg38UCSC Ensembl
Innerchr6:162775855..162888704hg19UCSC Ensembl
Innerchr6:162695845..162808694hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38112850
hg19112850
hg18112850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11019n54
Supporting Variantsnssv1075555, nssv1075554
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605156
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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