A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9669613



Internal ID13370662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74160226..74160245hg38UCSC Ensembl
Innerchr15:74160222..74160249hg38UCSC Ensembl
Outerchr15:74160203..74160268hg38UCSC Ensembl
chr15:74452567..74452586hg19UCSC Ensembl
Innerchr15:74452563..74452590hg19UCSC Ensembl
Outerchr15:74452544..74452609hg19UCSC Ensembl
chr15:72239620..72239639hg18UCSC Ensembl
Innerchr15:72239643..72239616hg18UCSC Ensembl
Outerchr15:72239597..72239662hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3400760
Supporting Variants
SamplesNA12045
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9669613
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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