A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7770667



Internal ID13606564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82882870..82882871hg38UCSC Ensembl
Innerchr15:82882853..82882883hg38UCSC Ensembl
Outerchr15:82882852..82882883hg38UCSC Ensembl
chr15:83551622..83551623hg19UCSC Ensembl
Innerchr15:83551605..83557690hg19UCSC Ensembl
Outerchr15:83551604..83557691hg19UCSC Ensembl
chr15:81348676..81348677hg18UCSC Ensembl
Innerchr15:81348694..81348659hg18UCSC Ensembl
Outerchr15:81348658..81348695hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386062
hg196062
hg186062
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3305212
Supporting Variants
SamplesNA12815
Known GenesHOMER2
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7770667
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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