A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7838662



Internal ID15007308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12101881..12101882hg38UCSC Ensembl
Innerchr6:12101813..12101950hg38UCSC Ensembl
Outerchr6:12101812..12101951hg38UCSC Ensembl
chr6:12102114..12102115hg19UCSC Ensembl
Innerchr6:12102046..12102183hg19UCSC Ensembl
Outerchr6:12102045..12102184hg19UCSC Ensembl
chr6:12210100..12210101hg18UCSC Ensembl
Innerchr6:12210169..12210032hg18UCSC Ensembl
Outerchr6:12210031..12210170hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38275
hg19275
hg18275
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3309155
Supporting Variants
SamplesNA19238
Known GenesHIVEP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7838662
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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