A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644488



Internal ID7031243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44567966..44575267hg38UCSC Ensembl
Innerchr19:44567980..44575253hg38UCSC Ensembl
Outerchr19:44567952..44575281hg38UCSC Ensembl
chr19:45071212..45078515hg19UCSC Ensembl
Innerchr19:45071226..45078501hg19UCSC Ensembl
Outerchr19:45071198..45078529hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg387302
hg197304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16064850
SamplesHG02855
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644488
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