A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009755



Internal ID15957025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157028236..157171909hg38UCSC Ensembl
Innerchr4:157949388..158093061hg19UCSC Ensembl
Innerchr4:158168838..158312511hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38143674
hg19143674
hg18143674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595803
Supporting Variants
Samples
Known GenesGLRB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1009755
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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