A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6166994



Internal ID9144397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10978761..10981046hg38UCSC Ensembl
Outerchr6:10978724..10981096hg38UCSC Ensembl
Innerchr6:10978994..10981279hg19UCSC Ensembl
Outerchr6:10978957..10981329hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg382373
hg192373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661047
Supporting Variants
SamplesNA19468
Known GenesELOVL2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6166994
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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