A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636223



Internal ID7023019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40119789..40130682hg38UCSC Ensembl
Innerchr15:40120289..40130182hg38UCSC Ensembl
Outerchr15:40118789..40131682hg38UCSC Ensembl
chr15:40411990..40422883hg19UCSC Ensembl
Innerchr15:40412490..40422383hg19UCSC Ensembl
Outerchr15:40410990..40423883hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3810894
hg1910894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15227732
SamplesNA20514
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636223
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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