A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779776



Internal ID19166557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102142172..102215271hg38UCSC Ensembl
Innerchr9:104904454..104977553hg19UCSC Ensembl
Innerchr9:103944275..104017374hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3873100
hg1973100
hg1873100
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891698
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=31
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779776
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