A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6424455



Internal ID8837576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3711218..3711824hg38UCSC Ensembl
Outerchr19:3710747..3712194hg38UCSC Ensembl
Innerchr19:3711216..3711822hg19UCSC Ensembl
Outerchr19:3710745..3712192hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381448
hg191448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669742
Supporting Variants
SamplesHG00275
Known GenesTJP3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6424455
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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