A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094786



Internal ID15947972
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 StatusS
Merged Variantsnsv608461
Supporting Variants
Samples
Known GenesCNOT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094786
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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