A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8673152



Internal ID15032417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36347952..36348020hg38UCSC Ensembl
Innerchr15:36347956..36348014hg38UCSC Ensembl
Outerchr15:36347888..36348082hg38UCSC Ensembl
chr15:36640153..36640221hg19UCSC Ensembl
Innerchr15:36640157..36640215hg19UCSC Ensembl
Outerchr15:36640089..36640283hg19UCSC Ensembl
chr15:34427445..34427513hg18UCSC Ensembl
Innerchr15:34427507..34427449hg18UCSC Ensembl
Outerchr15:34427381..34427575hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38133
hg19133
hg18133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3430841
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8673152
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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