A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893011



Internal ID19183831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:39162776..39170912hg38UCSC Ensembl
Outerchr17:39160735..39172813hg38UCSC Ensembl
Innerchr17:37319029..37327165hg19UCSC Ensembl
Outerchr17:37316988..37329066hg19UCSC Ensembl
Innerchr17:34572555..34580691hg18UCSC Ensembl
Outerchr17:34570514..34582592hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3812079
hg1912079
hg1812079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787431, essv25797514, essv25796194, essv25783351, essv25786168, essv25780878, essv25786564, essv25798884, essv25801374, essv25780248, essv25801597, essv25801545, essv25786286
Samples
Known GenesARL5C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893011
Frequency
Sample Size3017
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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