A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595683



Internal ID16383092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148444757..148445719hg38UCSC Ensembl
Innerchr4:149365909..149366871hg19UCSC Ensembl
Innerchr4:149585359..149586321hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38963
hg19963
hg18963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9311n54
Supporting Variantsnssv1009398
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595683
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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