A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600806



Internal ID16388215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1577201..1597922hg38UCSC Ensembl
Innerchr6:1577436..1598157hg19UCSC Ensembl
Innerchr6:1522435..1543156hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3820722
hg1920722
hg1820722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154018
Samples1780862414_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600806
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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