A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796350



Internal ID19167499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:81143961..81187865hg38UCSC Ensembl
Innerchr13:81718096..81762000hg19UCSC Ensembl
Innerchr13:80616097..80660001hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3843905
hg1943905
hg1843905
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892397
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796350
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