A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012383



Internal ID19101600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34759898..34823091hg38UCSC Ensembl
Innerchr4:34761520..34824713hg19UCSC Ensembl
Innerchr4:34437915..34501108hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3863194
hg1963194
hg1863194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5167n100
Supporting Variantsnssv3737779, nssv3620670, nssv3620667, nssv3620668, nssv3620666, nssv3620671, nssv3620669, nssv3620665
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)nsv1012383
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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