A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892443



Internal ID19183263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107497872..107527542hg38UCSC Ensembl
Outerchr13:107497872..107527542hg38UCSC Ensembl
Innerchr13:108150220..108179890hg19UCSC Ensembl
Outerchr13:108150220..108179890hg19UCSC Ensembl
Innerchr13:106948221..106977891hg18UCSC Ensembl
Outerchr13:106948221..106977891hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3829671
hg1929671
hg1829671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784038, essv25801047
Samples
Known GenesFAM155A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892443
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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