A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037926



Internal ID19127145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4234887..4337814hg38UCSC Ensembl
Innerchr11:4256117..4359044hg19UCSC Ensembl
Innerchr11:4212693..4315620hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38102928
hg19102928
hg18102928
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1021n100
Supporting Variantsnssv3516634, nssv3706401, nssv3706399, nssv3509716, nssv3515814, nssv3505567, nssv3505826, nssv3507333, nssv3512257, nssv3506280, nssv3507123, nssv3706403, nssv3706404, nssv3706400, nssv3504270, nssv3513489, nssv3511547, nssv3502973, nssv3512809, nssv3519835, nssv3513297, nssv3521925, nssv3521706, nssv3517551, nssv3516056, nssv3518205, nssv3515630, nssv3509234, nssv3519397, nssv3706402, nssv3516532, nssv3508457, nssv3510790, nssv3503568, nssv3508513, nssv3510679, nssv3504439, nssv3514780, nssv3518686, nssv3510527, nssv3519102, nssv3520972, nssv3504882, nssv3514037, nssv3512269
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)nsv1037926
Frequency
Sample Size11257
Observed Gain15
Observed Loss30
Observed Complex0
Frequencyn/a


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