A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600850



Internal ID16388259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3610610..3621551hg38UCSC Ensembl
Innerchr6:3610844..3621785hg19UCSC Ensembl
Innerchr6:3555843..3566784hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3810942
hg1910942
hg1810942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1048692
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600850
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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