A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16041342



Internal ID6043158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32878182..32959595hg38UCSC Ensembl
Innerchr19:32878367..32959410hg38UCSC Ensembl
Outerchr19:32877997..32959780hg38UCSC Ensembl
chr19:33369088..33450501hg19UCSC Ensembl
Innerchr19:33369273..33450316hg19UCSC Ensembl
Outerchr19:33368903..33450686hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3881414
hg1981414
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644180
Supporting Variants
SamplesHG01125
Known GenesCEP89
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16041342
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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