A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8651924



Internal ID15100637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42624429..42624845hg38UCSC Ensembl
Innerchr15:42624429..42624845hg38UCSC Ensembl
Outerchr15:42623691..42625089hg38UCSC Ensembl
chr15:42916627..42917043hg19UCSC Ensembl
Innerchr15:42916627..42917043hg19UCSC Ensembl
Outerchr15:42915889..42917287hg19UCSC Ensembl
chr15:40703919..40704335hg18UCSC Ensembl
Innerchr15:40703919..40704335hg18UCSC Ensembl
Outerchr15:40703181..40704579hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38417
hg19417
hg18417
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3325908
Supporting Variants
SamplesNA19240
Known GenesSTARD9
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8651924
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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