A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636330



Internal ID7023124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45034816..45071562hg38UCSC Ensembl
Innerchr15:45034816..45071562hg38UCSC Ensembl
Outerchr15:45034316..45072062hg38UCSC Ensembl
chr15:45327014..45363760hg19UCSC Ensembl
Innerchr15:45327014..45363760hg19UCSC Ensembl
Outerchr15:45326514..45364260hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3836747
hg1936747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233726
SamplesHG03644
Known GenesSORD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636330
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