A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3415665



Internal ID15262624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34558636..34558636hg38UCSC Ensembl
Innerchr19:34558635..34558637hg38UCSC Ensembl
Outerchr19:34558586..34558686hg38UCSC Ensembl
chr19:35049541..35049541hg19UCSC Ensembl
Innerchr19:35049540..35049542hg19UCSC Ensembl
Outerchr19:35049491..35049591hg19UCSC Ensembl
chr19:39741381..39741381hg18UCSC Ensembl
Innerchr19:39741382..39741380hg18UCSC Ensembl
Outerchr19:39741331..39741431hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38877
hg19877
hg18877
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8740909
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3415665
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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