A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16069695



Internal ID3999127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46772338..46772973hg38UCSC Ensembl
Innerchr19:46772351..46772961hg38UCSC Ensembl
Outerchr19:46772326..46772986hg38UCSC Ensembl
chr19:47275595..47276230hg19UCSC Ensembl
Innerchr19:47275608..47276218hg19UCSC Ensembl
Outerchr19:47275583..47276243hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644537
Supporting Variants
SamplesHG03649
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16069695
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