A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9669480



Internal ID13246679
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 StatusS
Merged Variantsesv3378324
Supporting Variants
SamplesNA12812
Known GenesLRRC49
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9669480
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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