A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790929



Internal ID18819632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71620009..71849534hg38UCSC Ensembl
Innerchr11:71331055..71560580hg19UCSC Ensembl
Innerchr11:71008703..71238228hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38229526
hg19229526
hg18229526
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892025
Supporting Variants
Samples
Known GenesALG1L9P, DEFB108B, FAM86C1, ZNF705E
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790929
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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