A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053588



Internal ID19142807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4217176..4337814hg38UCSC Ensembl
Innerchr11:4238406..4359044hg19UCSC Ensembl
Innerchr11:4194982..4315620hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38120639
hg19120639
hg18120639
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1021n100
Supporting Variantsnssv3509654, nssv3522384, nssv3505432, nssv3509765
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)nsv1053588
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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