A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671224



Internal ID9937329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31681593..31737773hg38UCSC Ensembl
Outerchr11:31681554..31737834hg38UCSC Ensembl
Innerchr11:31703141..31759321hg19UCSC Ensembl
Outerchr11:31703102..31759382hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3856281
hg1956281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6278286
SamplesHG00131
Known GenesELP4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671224
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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