A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784119



Internal ID18813032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:101443165..101456121hg38UCSC Ensembl
Innerchr13:102095516..102108472hg19UCSC Ensembl
Innerchr13:100893517..100906473hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3812957
hg1912957
hg1812957
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892436
Supporting Variants
Samples
Known GenesITGBL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784119
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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