A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6367056



Internal ID9367038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127367274..127369382hg38UCSC Ensembl
Outerchr10:127367228..127369445hg38UCSC Ensembl
Innerchr10:129165538..129167646hg19UCSC Ensembl
Outerchr10:129165492..129167709hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382218
hg192218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676964
Supporting Variants
SamplesNA18561
Known GenesDOCK1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6367056
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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