A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3446736



Internal ID15293686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164925573..164926571hg38UCSC Ensembl
Innerchr6:164925572..164926572hg38UCSC Ensembl
Outerchr6:164924573..164927571hg38UCSC Ensembl
chr6:165339062..165340060hg19UCSC Ensembl
Innerchr6:165339061..165340061hg19UCSC Ensembl
Outerchr6:165338062..165341060hg19UCSC Ensembl
chr6:165259052..165260050hg18UCSC Ensembl
Innerchr6:165260051..165259051hg18UCSC Ensembl
Outerchr6:165258052..165261050hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38999
hg19999
hg18999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3706e59
Supporting Variantsessv8695089
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3446736
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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