A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6311238



Internal ID9233097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:129616..202022hg38UCSC Ensembl
Outerchr6:129245..202392hg38UCSC Ensembl
Innerchr6:129616..202022hg19UCSC Ensembl
Outerchr6:129245..202392hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3873148
hg1973148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669800
Supporting Variants
SamplesNA11920
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6311238
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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