A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8678125



Internal ID15103097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64118985..64119004hg38UCSC Ensembl
Innerchr15:64118981..64119008hg38UCSC Ensembl
Outerchr15:64118962..64119027hg38UCSC Ensembl
chr15:64411184..64411203hg19UCSC Ensembl
Innerchr15:64411180..64411207hg19UCSC Ensembl
Outerchr15:64411161..64411226hg19UCSC Ensembl
chr15:62198237..62198256hg18UCSC Ensembl
Innerchr15:62198260..62198233hg18UCSC Ensembl
Outerchr15:62198214..62198279hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3412562
Supporting Variants
SamplesNA19240
Known GenesSNX1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8678125
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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