A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605124



Internal ID16045847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162269602..162514399hg38UCSC Ensembl
Innerchr6:162690634..162935431hg19UCSC Ensembl
Innerchr6:162610624..162855421hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38244798
hg19244798
hg18244798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11013n54
Supporting Variantsnssv1075526
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605124
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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