A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605163



Internal ID16045886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162410304..162562811hg38UCSC Ensembl
Innerchr6:162831336..162983843hg19UCSC Ensembl
Innerchr6:162751326..162903833hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38152508
hg19152508
hg18152508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075561
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605163
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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