A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6394341



Internal ID9371744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3630637..3640995hg38UCSC Ensembl
chr11:3651867..3662225hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810359
hg1910359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658889
Supporting Variants
SamplesHG00707
Known GenesART5, TRPC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6394341
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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