A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891717



Internal ID18839427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113128729..113157819hg38UCSC Ensembl
Outerchr9:113128729..113157819hg38UCSC Ensembl
Innerchr9:115891009..115920099hg19UCSC Ensembl
Outerchr9:115891009..115920099hg19UCSC Ensembl
Innerchr9:114930830..114959920hg18UCSC Ensembl
Outerchr9:114930830..114959920hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3829091
hg1929091
hg1829091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784261
Samples
Known GenesSLC31A2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891717
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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