A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6594949



Internal ID9151347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34227828..34228153hg38UCSC Ensembl
chr11:34249375..34249700hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678936
Supporting Variants
SamplesHG01334
Known GenesABTB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6594949
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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