A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865801



Internal ID13318075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36113084..36113102hg38UCSC Ensembl
Innerchr15:36113086..36113100hg38UCSC Ensembl
Outerchr15:36113082..36113104hg38UCSC Ensembl
chr15:36405285..36405303hg19UCSC Ensembl
Innerchr15:36405287..36405301hg19UCSC Ensembl
Outerchr15:36405283..36405305hg19UCSC Ensembl
chr15:34192577..34192595hg18UCSC Ensembl
Innerchr15:34192579..34192593hg18UCSC Ensembl
Outerchr15:34192575..34192597hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3419526
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865801
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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