A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6563109



Internal ID9571821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38743016..38761722hg38UCSC Ensembl
Outerchr11:38742645..38762092hg38UCSC Ensembl
Innerchr11:38764566..38783272hg19UCSC Ensembl
Outerchr11:38764195..38783642hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3819448
hg1919448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660587
Supporting Variants
SamplesNA19130
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6563109
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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