A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038465



Internal ID19127684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4215479..4325567hg38UCSC Ensembl
Innerchr11:4236709..4346797hg19UCSC Ensembl
Innerchr11:4193285..4303373hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38110089
hg19110089
hg18110089
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1021n100
Supporting Variantsnssv3508834, nssv3504898, nssv3508659, nssv3511172
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)nsv1038465
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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