A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801047



Internal ID19172338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107497872..107527542hg38UCSC Ensembl
Innerchr13:108150220..108179890hg19UCSC Ensembl
Innerchr13:106948221..106977891hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3829671
hg1929671
hg1829671
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892443
Supporting Variants
Samples
Known GenesFAM155A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801047
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer