A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009397



Internal ID16303353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148444757..148445636hg38UCSC Ensembl
Innerchr4:149365909..149366788hg19UCSC Ensembl
Innerchr4:149585359..149586238hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38880
hg19880
hg18880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595682
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1009397
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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