A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9668836



Internal ID13606127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55324571..55324590hg38UCSC Ensembl
Innerchr15:55324567..55324594hg38UCSC Ensembl
Outerchr15:55324548..55324613hg38UCSC Ensembl
chr15:55616769..55616788hg19UCSC Ensembl
Innerchr15:55616765..55616792hg19UCSC Ensembl
Outerchr15:55616746..55616811hg19UCSC Ensembl
chr15:53404061..53404080hg18UCSC Ensembl
Innerchr15:53404084..53404057hg18UCSC Ensembl
Outerchr15:53404038..53404103hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3333010
Supporting Variants
SamplesNA12815
Known GenesPIGB
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9668836
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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