A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865438



Internal ID14646019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7015595..7015638hg38UCSC Ensembl
Innerchr11:7015537..7015696hg38UCSC Ensembl
Outerchr11:7015494..7015739hg38UCSC Ensembl
chr11:7036826..7036869hg19UCSC Ensembl
Innerchr11:7036768..7036927hg19UCSC Ensembl
Outerchr11:7036725..7036970hg19UCSC Ensembl
chr11:6993402..6993445hg18UCSC Ensembl
Innerchr11:6993503..6993344hg18UCSC Ensembl
Outerchr11:6993301..6993546hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3417932
Supporting Variants
SamplesNA18961
Known GenesZNF214
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865438
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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