A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605149



Internal ID16045872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162331661..162468943hg38UCSC Ensembl
Innerchr6:162752693..162889975hg19UCSC Ensembl
Innerchr6:162672683..162809965hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38137283
hg19137283
hg18137283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11019n54
Supporting Variantsnssv1075548
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605149
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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