A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602817



Internal ID16390226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32967732..32973437hg38UCSC Ensembl
Innerchr6:32935509..32941214hg19UCSC Ensembl
Innerchr6:33043487..33049192hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg385706
hg195706
hg185706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1057621
Samples
Known GenesBRD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602817
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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