A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3434666



Internal ID15281620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170736739..170745937hg38UCSC Ensembl
Innerchr6:170737739..170744937hg38UCSC Ensembl
Outerchr6:170735739..170745979hg38UCSC Ensembl
chr6:171045827..171055000hg19UCSC Ensembl
Innerchr6:171046827..171054025hg19UCSC Ensembl
Outerchr6:171044827..171055000hg19UCSC Ensembl
chr6:170887752..170896950hg18UCSC Ensembl
Innerchr6:170888752..170895950hg18UCSC Ensembl
Outerchr6:170886752..170897950hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg389199
hg199174
hg189199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3727e59
Supporting Variantsessv8695173
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3434666
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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