A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784654



Internal ID19175038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:102574418..102613741hg38UCSC Ensembl
Innerchr3:102293262..102332585hg19UCSC Ensembl
Innerchr3:103775952..103815275hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3839324
hg1939324
hg1839324
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893753
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784654
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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