A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007691



Internal ID19096910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34768672..34822549hg38UCSC Ensembl
Innerchr4:34770294..34824171hg19UCSC Ensembl
Innerchr4:34446689..34500566hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3853878
hg1953878
hg1853878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5167n100
Supporting Variantsnssv3620728, nssv3620729, nssv3620724, nssv3620726, nssv3737783, nssv3620731, nssv3620730, nssv3620727, nssv3620725
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)nsv1007691
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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