A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15986581



Internal ID5988397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6579137..6581947hg38UCSC Ensembl
Innerchr19:6579302..6581897hg38UCSC Ensembl
Outerchr19:6579017..6582067hg38UCSC Ensembl
chr19:6579148..6581958hg19UCSC Ensembl
Innerchr19:6579313..6581908hg19UCSC Ensembl
Outerchr19:6579028..6582078hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643561
Supporting Variants
SamplesNA21104
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15986581
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