A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7864561



Internal ID12970424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25838478..25838490hg38UCSC Ensembl
Innerchr6:25838480..25838488hg38UCSC Ensembl
Outerchr6:25838476..25838492hg38UCSC Ensembl
chr6:25838706..25838718hg19UCSC Ensembl
Innerchr6:25838708..25838716hg19UCSC Ensembl
Outerchr6:25838704..25838720hg19UCSC Ensembl
chr6:25946685..25946697hg18UCSC Ensembl
Innerchr6:25946687..25946695hg18UCSC Ensembl
Outerchr6:25946683..25946699hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3447143
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7864561
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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