A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6183386



Internal ID9160789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46399316..46401005hg38UCSC Ensembl
chr10:47148758..47150447hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381690
hg191690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668279
Supporting Variants
SamplesNA19440
Known GenesLINC00842
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6183386
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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