A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785872



Internal ID19167021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:67946181..67958062hg38UCSC Ensembl
Innerchr3:67996605..68008479hg19UCSC Ensembl
Innerchr3:68079295..68091169hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3811882
hg1911875
hg1811875
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893719
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785872
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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