A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8701305



Internal ID13642576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36132544..36132544hg38UCSC Ensembl
Innerchr15:36132543..36132545hg38UCSC Ensembl
Outerchr15:36132494..36132594hg38UCSC Ensembl
chr15:36424745..36424745hg19UCSC Ensembl
Innerchr15:36424744..36424746hg19UCSC Ensembl
Outerchr15:36424695..36424795hg19UCSC Ensembl
chr15:34212037..34212037hg18UCSC Ensembl
Innerchr15:34212038..34212036hg18UCSC Ensembl
Outerchr15:34211987..34212087hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38123
hg19123
hg18123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3336720
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8701305
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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