A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3435434



Internal ID14935702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167290774..167292572hg38UCSC Ensembl
Innerchr6:167291572..167291774hg38UCSC Ensembl
Outerchr6:167289774..167293572hg38UCSC Ensembl
chr6:167704262..167706060hg19UCSC Ensembl
Innerchr6:167705060..167705262hg19UCSC Ensembl
Outerchr6:167703262..167707060hg19UCSC Ensembl
chr6:167624252..167626050hg18UCSC Ensembl
Innerchr6:167625252..167625050hg18UCSC Ensembl
Outerchr6:167623252..167627050hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381799
hg191799
hg181799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8695104
SamplesNA19239
Known GenesUNC93A
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3435434
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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