A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3406827



Internal ID15253789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26751419..26751433hg38UCSC Ensembl
Innerchr10:26751415..26751435hg38UCSC Ensembl
Outerchr10:26751401..26751451hg38UCSC Ensembl
chr10:27040348..27040362hg19UCSC Ensembl
Innerchr10:27040344..27040364hg19UCSC Ensembl
Outerchr10:27040330..27040380hg19UCSC Ensembl
chr10:27080354..27080368hg18UCSC Ensembl
Innerchr10:27080370..27080350hg18UCSC Ensembl
Outerchr10:27080336..27080386hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8947647, essv8947636, essv8947645, essv8947637, essv8947644, essv8947639, essv8947649, essv8947638, essv8947642, essv8947641, essv8947640, essv8947634, essv8947633, essv8947648, essv8947643
SamplesNA19190, NA12155, NA18550, NA18582, NA12156, NA12003, NA18856, NA18523, NA18570, NA18576, NA18608, NA19108, NA19093, NA18609, NA12154
Known GenesABI1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3406827
Frequency
Sample Size185
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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