A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3434658



Internal ID15281612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85084532..85084551hg38UCSC Ensembl
Innerchr11:85084528..85084555hg38UCSC Ensembl
Outerchr11:85084509..85084574hg38UCSC Ensembl
chr11:84795576..84795595hg19UCSC Ensembl
Innerchr11:84795572..84795599hg19UCSC Ensembl
Outerchr11:84795553..84795618hg19UCSC Ensembl
chr11:84473224..84473243hg18UCSC Ensembl
Innerchr11:84473247..84473220hg18UCSC Ensembl
Outerchr11:84473201..84473266hg18UCSC Ensembl
Cytoband11q14.1
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 Variantsessv9653292
SamplesNA12815
Known GenesDLG2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3434658
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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