A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9668125



Internal ID14911202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36347960..36347979hg38UCSC Ensembl
Innerchr15:36347956..36347983hg38UCSC Ensembl
Outerchr15:36347937..36348002hg38UCSC Ensembl
chr15:36640161..36640180hg19UCSC Ensembl
Innerchr15:36640157..36640184hg19UCSC Ensembl
Outerchr15:36640138..36640203hg19UCSC Ensembl
chr15:34427453..34427472hg18UCSC Ensembl
Innerchr15:34427476..34427449hg18UCSC Ensembl
Outerchr15:34427430..34427495hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3427573
Supporting Variants
SamplesNA19141
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9668125
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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