A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6579678



Internal ID9788931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60803991..60804657hg38UCSC Ensembl
Outerchr11:60803954..60804707hg38UCSC Ensembl
Innerchr11:60571464..60572130hg19UCSC Ensembl
Outerchr11:60571427..60572180hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662808
Supporting Variants
SamplesNA19780
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6579678
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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