A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3378324



Internal ID14878593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70861397..70861416hg38UCSC Ensembl
Innerchr15:70861393..70861420hg38UCSC Ensembl
Outerchr15:70861374..70861439hg38UCSC Ensembl
chr15:71153736..71153755hg19UCSC Ensembl
Innerchr15:71153732..71153759hg19UCSC Ensembl
Outerchr15:71153713..71153778hg19UCSC Ensembl
chr15:68940790..68940809hg18UCSC Ensembl
Innerchr15:68940813..68940786hg18UCSC Ensembl
Outerchr15:68940767..68940832hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9669491, essv9669469, essv9669513, essv9669502, essv9669480
SamplesNA12812, NA12287, NA18970, NA12815, NA12249
Known GenesLRRC49
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3378324
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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