A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5781933



Internal ID8759336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60174839..60175213hg38UCSC Ensembl
chr11:59942312..59942686hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674897
Supporting Variants
SamplesHG01377
Known GenesMS4A6A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5781933
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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