A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3329051



Internal ID14829329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34536481..34750556hg38UCSC Ensembl
Innerchr19:34538471..34748976hg38UCSC Ensembl
Outerchr19:34536371..34750676hg38UCSC Ensembl
chr19:35027386..35241461hg19UCSC Ensembl
Innerchr19:35029376..35239881hg19UCSC Ensembl
Outerchr19:35027276..35241581hg19UCSC Ensembl
chr19:39719226..39933301hg18UCSC Ensembl
Innerchr19:39721216..39931721hg18UCSC Ensembl
Outerchr19:39719116..39933421hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38214076
hg19214076
hg18214076
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8808853
SamplesNA12878
Known GenesSCGB1B2P, SCGB2B2, SCGB2B3P, ZNF181, ZNF302
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3329051
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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