A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605091



Internal ID16045814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162163721..162165648hg38UCSC Ensembl
Innerchr6:162584753..162586680hg19UCSC Ensembl
Innerchr6:162504743..162506670hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381928
hg191928
hg181928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11007n54
Supporting Variantsnssv1075409, nssv1075410, nssv1075411
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605091
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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