A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605074



Internal ID16392483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161934723..161995173hg38UCSC Ensembl
Innerchr6:162355755..162416205hg19UCSC Ensembl
Innerchr6:162275745..162336195hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3860451
hg1960451
hg1860451
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075382
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605074
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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