A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3335094



Internal ID14835367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80808788..80808799hg38UCSC Ensembl
Innerchr15:80808793..80808794hg38UCSC Ensembl
Outerchr15:80808783..80808804hg38UCSC Ensembl
chr15:81101129..81101140hg19UCSC Ensembl
Innerchr15:81101134..81101135hg19UCSC Ensembl
Outerchr15:81101124..81101145hg19UCSC Ensembl
chr15:78888184..78888195hg18UCSC Ensembl
Innerchr15:78888189..78888190hg18UCSC Ensembl
Outerchr15:78888179..78888200hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865830
SamplesNA12005
Known GenesKIAA1199
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3335094
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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