A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3405692



Internal ID15252654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43867600..43867619hg38UCSC Ensembl
Innerchr15:43867596..43867623hg38UCSC Ensembl
Outerchr15:43867577..43867642hg38UCSC Ensembl
chr15:44159798..44159817hg19UCSC Ensembl
Innerchr15:44159794..44159821hg19UCSC Ensembl
Outerchr15:44159775..44159840hg19UCSC Ensembl
chr15:41947090..41947109hg18UCSC Ensembl
Innerchr15:41947113..41947086hg18UCSC Ensembl
Outerchr15:41947067..41947132hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg386000
hg196000
hg186000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9668380
SamplesNA12873
Known GenesWDR76
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3405692
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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