A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606859



Internal ID16394268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:47346824..47384489hg38UCSC Ensembl
Innerchr7:47386422..47424086hg19UCSC Ensembl
Innerchr7:47352947..47390611hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3837666
hg1937665
hg1837665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1083683
Samples
Known GenesTNS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606859
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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