A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779768



Internal ID19169932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90350411..90432319hg38UCSC Ensembl
Innerchr13:91002665..91084573hg19UCSC Ensembl
Innerchr13:89800666..89882574hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3881909
hg1981909
hg1881909
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892421
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=25
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779768
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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