A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643677



Internal ID6683748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11804145..11953016hg38UCSC Ensembl
Innerchr19:11804295..11952866hg38UCSC Ensembl
Outerchr19:11803995..11953166hg38UCSC Ensembl
chr19:11914960..12063831hg19UCSC Ensembl
Innerchr19:11915110..12063681hg19UCSC Ensembl
Outerchr19:11914810..12063981hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38148872
hg19148872
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15991044
SamplesHG00109
Known GenesZNF439, ZNF440, ZNF491, ZNF69, ZNF700
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643677
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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