A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7765992



Internal ID13617678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77469237..77469238hg38UCSC Ensembl
Innerchr15:77469215..77469260hg38UCSC Ensembl
Outerchr15:77469214..77469261hg38UCSC Ensembl
chr15:77761579..77761580hg19UCSC Ensembl
Innerchr15:77761557..77761602hg19UCSC Ensembl
Outerchr15:77761556..77761603hg19UCSC Ensembl
chr15:75548634..75548635hg18UCSC Ensembl
Innerchr15:75548657..75548612hg18UCSC Ensembl
Outerchr15:75548611..75548658hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38292
hg19292
hg18292
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3306898
Supporting Variants
SamplesNA12873
Known GenesHMG20A
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7765992
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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