A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000435



Internal ID19089652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25555425..25584584hg38UCSC Ensembl
Innerchr4:25557047..25586206hg19UCSC Ensembl
Innerchr4:25166145..25195304hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3829160
hg1929160
hg1829160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5160n100
Supporting Variantsnssv3620606
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000435
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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