A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051879



Internal ID18794410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71588129..71825814hg38UCSC Ensembl
Innerchr11:71299175..71536860hg19UCSC Ensembl
Innerchr11:70976823..71214508hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38237686
hg19237686
hg18237686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1222n100
Supporting Variantsnssv3710646, nssv3710645, nssv3710647
Samples
Known GenesALG1L9P, FAM86C1, ZNF705E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051879
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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