A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893749



Internal ID19184569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95905623..95994505hg38UCSC Ensembl
Outerchr3:95905623..95994505hg38UCSC Ensembl
Innerchr3:95624467..95713349hg19UCSC Ensembl
Outerchr3:95624467..95713349hg19UCSC Ensembl
Innerchr3:97107157..97196039hg18UCSC Ensembl
Outerchr3:97107157..97196039hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3888883
hg1988883
hg1888883
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792010, essv25789551
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893749
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer