A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7805910



Internal ID14780531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19361209..19361210hg38UCSC Ensembl
Innerchr11:19361191..19361228hg38UCSC Ensembl
Outerchr11:19361190..19361229hg38UCSC Ensembl
chr11:19382756..19382757hg19UCSC Ensembl
Innerchr11:19382738..19382775hg19UCSC Ensembl
Outerchr11:19382737..19382776hg19UCSC Ensembl
chr11:19339332..19339333hg18UCSC Ensembl
Innerchr11:19339351..19339314hg18UCSC Ensembl
Outerchr11:19339313..19339352hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38305
hg19305
hg18305
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3307077
Supporting Variants
SamplesNA19257
Known GenesNAV2
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7805910
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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