A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9667958



Internal ID13271063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32821087..32821106hg38UCSC Ensembl
Innerchr15:32821083..32821110hg38UCSC Ensembl
Outerchr15:32821064..32821129hg38UCSC Ensembl
chr15:33113288..33113307hg19UCSC Ensembl
Innerchr15:33113284..33113311hg19UCSC Ensembl
Outerchr15:33113265..33113330hg19UCSC Ensembl
chr15:30900580..30900599hg18UCSC Ensembl
Innerchr15:30900603..30900576hg18UCSC Ensembl
Outerchr15:30900557..30900622hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3365060
Supporting Variants
SamplesNA12873
Known GenesFMN1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9667958
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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