A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006183



Internal ID19095401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34759898..34819706hg38UCSC Ensembl
Innerchr4:34761520..34821328hg19UCSC Ensembl
Innerchr4:34437915..34497723hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3859809
hg1959809
hg1859809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5167n100
Supporting Variantsnssv3620663, nssv3620662, nssv3620659, nssv3620661, nssv3620664, nssv3620660
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)nsv1006183
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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