A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8695019



Internal ID15089440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11319133..11320031hg38UCSC Ensembl
Innerchr6:11319132..11320032hg38UCSC Ensembl
Outerchr6:11318133..11321031hg38UCSC Ensembl
chr6:11319366..11320264hg19UCSC Ensembl
Innerchr6:11319365..11320265hg19UCSC Ensembl
Outerchr6:11318366..11321264hg19UCSC Ensembl
chr6:11427352..11428250hg18UCSC Ensembl
Innerchr6:11428251..11427351hg18UCSC Ensembl
Outerchr6:11426352..11429250hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3360064
Supporting Variants
SamplesNA19240
Known GenesNEDD9
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8695019
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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