A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013715



Internal ID19102934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..36755hg38UCSC Ensembl
Innerchr4:12269..36756hg19UCSC Ensembl
Innerchr4:2269..26756hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3824487
hg1924488
hg1824488
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5050n100
Supporting Variantsnssv3737899, nssv3737898, nssv3737912, nssv3737906, nssv3737894, nssv3737888, nssv3737889, nssv3617064, nssv3617071, nssv3617098, nssv3617073, nssv3617092, nssv3737897, nssv3617087, nssv3737887, nssv3737893, nssv3617070, nssv3737890, nssv3617079, nssv3617090, nssv3617091, nssv3737902, nssv3617096, nssv3617078, nssv3737915, nssv3617085, nssv3737908, nssv3617086, nssv3617076, nssv3737909, nssv3617068, nssv3737891, nssv3617102, nssv3617094, nssv3617077, nssv3617093, nssv3617103, nssv3737896, nssv3737892, nssv3617099, nssv3617101, nssv3737907, nssv3737895, nssv3737911, nssv3737901, nssv3617067, nssv3617072, nssv3617065, nssv3737905, nssv3617088, nssv3737910, nssv3617083, nssv3617095, nssv3617084, nssv3737904, nssv3617069, nssv3617075, nssv3617089, nssv3617081, nssv3617082, nssv3617074, nssv3617066, nssv3737900, nssv3617097, nssv3737903, nssv3737913, nssv3737914, nssv3617100, nssv3617080
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)nsv1013715
Frequency
Sample Size11257
Observed Gain50
Observed Loss19
Observed Complex0
Frequencyn/a


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