A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8701306



Internal ID13295894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39891207..39891207hg38UCSC Ensembl
Innerchr15:39891206..39891208hg38UCSC Ensembl
Outerchr15:39891157..39891257hg38UCSC Ensembl
chr15:40183408..40183408hg19UCSC Ensembl
Innerchr15:40183407..40183409hg19UCSC Ensembl
Outerchr15:40183358..40183458hg19UCSC Ensembl
chr15:37970700..37970700hg18UCSC Ensembl
Innerchr15:37970701..37970699hg18UCSC Ensembl
Outerchr15:37970650..37970750hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38491
hg19491
hg18491
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3333387
Supporting Variants
SamplesNA12878
Known GenesGPR176
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8701306
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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