A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004235



Internal ID19093452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..52484hg38UCSC Ensembl
Innerchr4:12269..52378hg19UCSC Ensembl
Innerchr4:2269..42378hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3840216
hg1940110
hg1840110
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5053n100
Supporting Variantsnssv3619268, nssv3619289, nssv3619312, nssv3619297, nssv3619270, nssv3619300, nssv3619314, nssv3737926, nssv3619323, nssv3619325, nssv3619324, nssv3619313, nssv3619277, nssv3619298, nssv3619316, nssv3619291, nssv3619279, nssv3619271, nssv3619311, nssv3619286, nssv3619317, nssv3619285, nssv3619304, nssv3619295, nssv3737928, nssv3619290, nssv3619275, nssv3619303, nssv3619278, nssv3619296, nssv3619287, nssv3619308, nssv3737927, nssv3619322, nssv3619318, nssv3619320, nssv3619294, nssv3619315, nssv3619262, nssv3619305, nssv3619265, nssv3619309, nssv3619307, nssv3619283, nssv3619288, nssv3619264, nssv3619266, nssv3619267, nssv3619284, nssv3619274, nssv3619321, nssv3619269, nssv3619280, nssv3619281, nssv3619310, nssv3737925, nssv3619263, nssv3619306, nssv3619293, nssv3619301, nssv3619273, nssv3619292, nssv3619282, nssv3619276, nssv3619302, nssv3619299, nssv3619272, nssv3619319
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)nsv1004235
Frequency
Sample Size11257
Observed Gain45
Observed Loss23
Observed Complex0
Frequencyn/a


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