A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047828



Internal ID18790359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93153482..93181889hg38UCSC Ensembl
Innerchr11:92886648..92915055hg19UCSC Ensembl
Innerchr11:92526296..92554703hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3828408
hg1928408
hg1828408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1253n100
Supporting Variantsnssv3514335
Samples
Known GenesSLC36A4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047828
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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