A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891713



Internal ID18839423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113026427..113104996hg38UCSC Ensembl
Outerchr9:113026427..113104996hg38UCSC Ensembl
Innerchr9:115788707..115867276hg19UCSC Ensembl
Outerchr9:115788707..115867276hg19UCSC Ensembl
Innerchr9:114828528..114907097hg18UCSC Ensembl
Outerchr9:114828528..114907097hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3878570
hg1978570
hg1878570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779144
Samples
Known GenesFAM225B, ZFP37
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891713
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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