A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637377



Internal ID7024170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97384670..97388080hg38UCSC Ensembl
Innerchr15:97384672..97388079hg38UCSC Ensembl
Outerchr15:97384669..97388082hg38UCSC Ensembl
chr15:97927900..97931310hg19UCSC Ensembl
Innerchr15:97927902..97931309hg19UCSC Ensembl
Outerchr15:97927899..97931312hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg383411
hg193411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15333423
SamplesHG04229
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637377
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