A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6110777



Internal ID9090264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:129999339..130001150hg38UCSC Ensembl
Outerchr6:129999182..130001303hg38UCSC Ensembl
Innerchr6:130320484..130322295hg19UCSC Ensembl
Outerchr6:130320327..130322448hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg382122
hg192122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662123
Supporting Variants
SamplesHG01070
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6110777
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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