A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1011004



Internal ID7074955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146787666..146787716hg38UCSC Ensembl
chr6:147108802..147108852hg19UCSC Ensembl
chr6:147150495..147150545hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3582308
SamplesHuRef
Known GenesADGB
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1011004
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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