A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15256365



Internal ID2534686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55484284..55490748hg38UCSC Ensembl
Innerchr15:55484434..55490598hg38UCSC Ensembl
Outerchr15:55484134..55490898hg38UCSC Ensembl
chr15:55776482..55782946hg19UCSC Ensembl
Innerchr15:55776632..55782796hg19UCSC Ensembl
Outerchr15:55776332..55783096hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386465
hg196465
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636565
Supporting Variants
SamplesHG02253
Known GenesDYX1C1, DYX1C1-CCPG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15256365
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