A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527077



Internal ID15107684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168843480..168845444hg38UCSC Ensembl
Innerchr4:169764631..169766595hg19UCSC Ensembl
Innerchr4:170001206..170003170hg18UCSC Ensembl
Innerchr4:170139361..170141325hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381965
hg191965
hg181965
hg171965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703456
Samples
Known GenesPALLD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527077
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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