A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999420



Internal ID19158957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68570842..68623605hg38UCSC Ensembl
Innerchr4:69436560..69489323hg19UCSC Ensembl
Innerchr4:69119155..69171918hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3852764
hg1952764
hg1852764
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5283n100
Supporting Variantsnssv3628962, nssv3628954, nssv3628963, nssv3628960, nssv3628956, nssv3628965, nssv3628957, nssv3628964, nssv3628961, nssv3628955, nssv3628959, nssv3628958
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)nsv999420
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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