A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046642



Internal ID18789173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133926415..133955026hg38UCSC Ensembl
Innerchr11:133796310..133824921hg19UCSC Ensembl
Innerchr11:133301520..133330131hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3828612
hg1928612
hg1828612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1301n100
Supporting Variantsnssv3510708, nssv3512479, nssv3506055, nssv3520987, nssv3509146
Samples
Known GenesIGSF9B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046642
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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