A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9669680



Internal ID13618299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77469241..77469260hg38UCSC Ensembl
Innerchr15:77469237..77469264hg38UCSC Ensembl
Outerchr15:77469218..77469283hg38UCSC Ensembl
chr15:77761583..77761602hg19UCSC Ensembl
Innerchr15:77761579..77761606hg19UCSC Ensembl
Outerchr15:77761560..77761625hg19UCSC Ensembl
chr15:75548638..75548657hg18UCSC Ensembl
Innerchr15:75548661..75548634hg18UCSC Ensembl
Outerchr15:75548615..75548680hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3362224
Supporting Variants
SamplesNA12873
Known GenesHMG20A
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9669680
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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