A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3405176



Internal ID15252138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51891703..51891724hg38UCSC Ensembl
Innerchr15:51891708..51891719hg38UCSC Ensembl
Outerchr15:51891687..51891740hg38UCSC Ensembl
chr15:52183900..52183921hg19UCSC Ensembl
Innerchr15:52183905..52183916hg19UCSC Ensembl
Outerchr15:52183884..52183937hg19UCSC Ensembl
chr15:49971192..49971213hg18UCSC Ensembl
Innerchr15:49971208..49971197hg18UCSC Ensembl
Outerchr15:49971176..49971229hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38215
hg19215
hg18215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8968239, essv8968236, essv8968241, essv8968238, essv8968235, essv8968240
SamplesNA11920, NA18558, NA18579, NA18948, NA18961, NA18609
Known GenesTMOD3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3405176
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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