A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6306441



Internal ID9086496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9186241..9189185hg38UCSC Ensembl
Outerchr10:9186084..9189363hg38UCSC Ensembl
Innerchr10:9228204..9231148hg19UCSC Ensembl
Outerchr10:9228047..9231326hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383280
hg193280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657306
Supporting Variants
SamplesHG01067
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6306441
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