A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002989



Internal ID19092206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25554550..25576647hg38UCSC Ensembl
Innerchr4:25556172..25578269hg19UCSC Ensembl
Innerchr4:25165270..25187367hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3822098
hg1922098
hg1822098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5159n100
Supporting Variantsnssv3737761, nssv3737762, nssv3737763, nssv3620603, nssv3620604, nssv3737760, nssv3620605, nssv3737759
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)nsv1002989
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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