A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605123



Internal ID16045846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162260712..162303215hg38UCSC Ensembl
Innerchr6:162681744..162724247hg19UCSC Ensembl
Innerchr6:162601734..162644237hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3842504
hg1942504
hg1842504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075525
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605123
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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