A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8695106



Internal ID14743814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167337574..167338672hg38UCSC Ensembl
Innerchr6:167337672..167338574hg38UCSC Ensembl
Outerchr6:167336574..167339672hg38UCSC Ensembl
chr6:167751062..167752160hg19UCSC Ensembl
Innerchr6:167751160..167752062hg19UCSC Ensembl
Outerchr6:167750062..167753160hg19UCSC Ensembl
chr6:167671052..167672150hg18UCSC Ensembl
Innerchr6:167672052..167671150hg18UCSC Ensembl
Outerchr6:167670052..167673150hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3361184
Supporting Variants
SamplesNA19240
Known GenesTTLL2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8695106
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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