A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892622



Internal ID19183442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23025556..23076472hg38UCSC Ensembl
Outerchr15:22963861..23121326hg38UCSC Ensembl
Innerchr15:22796596..22847512hg19UCSC Ensembl
Outerchr15:22751742..22909207hg19UCSC Ensembl
Innerchr15:20347960..20398953hg18UCSC Ensembl
Outerchr15:20303106..20460648hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38157466
hg19157466
hg18157543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789039, essv25788405, essv25790868
Samples
Known GenesCYFIP1, TUBGCP5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892622
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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