A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605103



Internal ID16045826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162164060..162165648hg38UCSC Ensembl
Innerchr6:162585092..162586680hg19UCSC Ensembl
Innerchr6:162505082..162506670hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381589
hg191589
hg181589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11007n54
Supporting Variantsnssv1075498, nssv1075497
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605103
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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