A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605176



Internal ID16045899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162559871..162658886hg38UCSC Ensembl
Innerchr6:162980903..163079918hg19UCSC Ensembl
Innerchr6:162900893..162999908hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3899016
hg1999016
hg1899016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075573
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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