A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608461



Internal ID16395870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135478179..135543514hg38UCSC Ensembl
Innerchr7:135162927..135228262hg19UCSC Ensembl
Innerchr7:134813467..134878802hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3865336
hg1965336
hg1865336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1094786
Samples
Known GenesCNOT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608461
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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