A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6125299



Internal ID9102702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73203051..73203990hg38UCSC Ensembl
chr11:72914096..72915035hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669809
Supporting Variants
SamplesNA19377
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6125299
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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