A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051627



Internal ID18794158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1576899..1697036hg38UCSC Ensembl
Innerchr11:1598129..1718266hg19UCSC Ensembl
Innerchr11:1554705..1674842hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38120138
hg19120138
hg18120138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520556
Samples
Known GenesFAM99A, FAM99B, KRTAP5-1, KRTAP5-2, KRTAP5-3, KRTAP5-4, KRTAP5-5, KRTAP5-AS1, MOB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051627
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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