A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643516



Internal ID6683587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4871424..4876686hg38UCSC Ensembl
Innerchr19:4871459..4876651hg38UCSC Ensembl
Outerchr19:4871389..4876721hg38UCSC Ensembl
chr19:4871436..4876698hg19UCSC Ensembl
Innerchr19:4871471..4876663hg19UCSC Ensembl
Outerchr19:4871401..4876733hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385263
hg195263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15982253
SamplesHG03777
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643516
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