A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16041335



Internal ID6043151
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644177
Supporting Variants
SamplesHG02031
Known GenesTDRD12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16041335
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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