A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6070783



Internal ID9756517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76396649..76400379hg38UCSC Ensembl
Outerchr11:76396612..76400429hg38UCSC Ensembl
Innerchr11:76107693..76111423hg19UCSC Ensembl
Outerchr11:76107656..76111473hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg383818
hg193818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664049
Supporting Variants
SamplesNA19711
Known GenesLOC100506127
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6070783
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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