A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892661



Internal ID19183481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32393132..32776080hg38UCSC Ensembl
Outerchr15:32393132..32776080hg38UCSC Ensembl
Innerchr15:32685333..33068281hg19UCSC Ensembl
Outerchr15:32685333..33068281hg19UCSC Ensembl
Innerchr15:30472625..30855573hg18UCSC Ensembl
Outerchr15:30472625..30855573hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38382949
hg19382949
hg18382949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792145
Samples
Known GenesARHGAP11A, FMN1, GOLGA8K, GOLGA8O, GOLGA8R, GREM1, LOC100131315, LOC100996255, SCG5, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892661
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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