A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048822



Internal ID18791353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67743143..67964843hg38UCSC Ensembl
Innerchr11:67510614..67732314hg19UCSC Ensembl
Innerchr11:67267190..67488890hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38221701
hg19221701
hg18221701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1219n100
Supporting Variantsnssv3519635
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048822
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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