A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605115



Internal ID16045838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162185048..162270386hg38UCSC Ensembl
Innerchr6:162606080..162691418hg19UCSC Ensembl
Innerchr6:162526070..162611408hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3885339
hg1985339
hg1885339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11010n54
Supporting Variantsnssv1075518
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605115
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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