A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025113



Internal ID19114331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132648215..132685086hg38UCSC Ensembl
Innerchr4:133569370..133606241hg19UCSC Ensembl
Innerchr4:133788820..133825691hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3836872
hg1936872
hg1836872
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639522
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)nsv1025113
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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