A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605102



Internal ID16045825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162164060..162165585hg38UCSC Ensembl
Innerchr6:162585092..162586617hg19UCSC Ensembl
Innerchr6:162505082..162506607hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381526
hg191526
hg181526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11007n54
Supporting Variantsnssv1075495, nssv1075494, nssv1075496
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605102
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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