A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644489



Internal ID7031244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44606502..44609423hg38UCSC Ensembl
Innerchr19:44606523..44609402hg38UCSC Ensembl
Outerchr19:44606481..44609444hg38UCSC Ensembl
chr19:45109819..45112741hg19UCSC Ensembl
Innerchr19:45109840..45112720hg19UCSC Ensembl
Outerchr19:45109798..45112762hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg382922
hg192923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv664e214
Supporting Variantsessv16064851
SamplesNA19023
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644489
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