A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892642



Internal ID18836776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30194842..30389978hg38UCSC Ensembl
Outerchr15:30194842..30491379hg38UCSC Ensembl
Innerchr15:30487045..30682181hg19UCSC Ensembl
Outerchr15:30487045..30783582hg19UCSC Ensembl
Innerchr15:28274337..28469473hg18UCSC Ensembl
Outerchr15:28274337..28570874hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38296538
hg19296538
hg18296538
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798686, essv25792616
Samples
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892642
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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