A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3430110



Internal ID15277066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43313163..43313182hg38UCSC Ensembl
Innerchr6:43313159..43313186hg38UCSC Ensembl
Outerchr6:43313140..43313205hg38UCSC Ensembl
chr6:43280901..43280920hg19UCSC Ensembl
Innerchr6:43280897..43280924hg19UCSC Ensembl
Outerchr6:43280878..43280943hg19UCSC Ensembl
chr6:43388879..43388898hg18UCSC Ensembl
Innerchr6:43388902..43388875hg18UCSC Ensembl
Outerchr6:43388856..43388921hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9627114
SamplesNA19141
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3430110
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer