A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003534



Internal ID19092752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34771881..34823091hg38UCSC Ensembl
Innerchr4:34773503..34824713hg19UCSC Ensembl
Innerchr4:34449898..34501108hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3851211
hg1951211
hg1851211
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5167n100
Supporting Variantsnssv3620847, nssv3737790, nssv3620831, nssv3620834, nssv3620849, nssv3737791, nssv3620852, nssv3620842, nssv3620837, nssv3620843, nssv3620838, nssv3620839, nssv3620851, nssv3620832, nssv3620845, nssv3620846, nssv3620840, nssv3620848, nssv3620836, nssv3620835, nssv3620853, nssv3620844, nssv3620841, nssv3620833, nssv3620850
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)nsv1003534
Frequency
Sample Size11257
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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