A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644177



Internal ID6684245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32717978..32732982hg38UCSC Ensembl
Innerchr19:32717978..32732982hg38UCSC Ensembl
Outerchr19:32717625..32733269hg38UCSC Ensembl
chr19:33208884..33223888hg19UCSC Ensembl
Innerchr19:33208884..33223888hg19UCSC Ensembl
Outerchr19:33208531..33224175hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3815005
hg1915005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16041335, essv16041336
SamplesHG02031, NA11892
Known GenesTDRD12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644177
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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