A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637387



Internal ID7024180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97877569..97878712hg38UCSC Ensembl
Innerchr15:97877569..97878712hg38UCSC Ensembl
Outerchr15:97877384..97878933hg38UCSC Ensembl
chr15:98420799..98421942hg19UCSC Ensembl
Innerchr15:98420799..98421942hg19UCSC Ensembl
Outerchr15:98420614..98422163hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381144
hg191144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15333886, essv15333885, essv15333884
SamplesHG00457, HG02383, HG02047
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637387
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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