A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605179



Internal ID16045902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162608811..162647813hg38UCSC Ensembl
Innerchr6:163029843..163068845hg19UCSC Ensembl
Innerchr6:162949833..162988835hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3839003
hg1939003
hg1839003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075575
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605179
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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