A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891968



Internal ID19186364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40750940..40924900hg38UCSC Ensembl
Outerchr11:40750940..40924900hg38UCSC Ensembl
Innerchr11:40772490..40946450hg19UCSC Ensembl
Outerchr11:40772490..40946450hg19UCSC Ensembl
Innerchr11:40729066..40903026hg18UCSC Ensembl
Outerchr11:40729066..40903026hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38173961
hg19173961
hg18173961
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792708
Samples
Known GenesLRRC4C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891968
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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