A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3391998



Internal ID15238963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70279459..70280657hg38UCSC Ensembl
Innerchr15:70279657..70280459hg38UCSC Ensembl
Outerchr15:70278459..70281657hg38UCSC Ensembl
chr15:70571798..70572996hg19UCSC Ensembl
Innerchr15:70571996..70572798hg19UCSC Ensembl
Outerchr15:70570798..70573996hg19UCSC Ensembl
chr15:68358852..68360050hg18UCSC Ensembl
Innerchr15:68359852..68359050hg18UCSC Ensembl
Outerchr15:68357852..68361050hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1441e59
Supporting Variantsessv8689780
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3391998
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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