A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006387



Internal ID19095604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34777226..34828370hg38UCSC Ensembl
Innerchr4:34778848..34829992hg19UCSC Ensembl
Innerchr4:34455243..34506387hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3851145
hg1951145
hg1851145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5167n100
Supporting Variantsnssv3619125, nssv3619130, nssv3619123, nssv3619129, nssv3619127, nssv3619128, nssv3619122, nssv3619124, nssv3619126
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)nsv1006387
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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