A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636333



Internal ID6676440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45097911..45101545hg38UCSC Ensembl
Innerchr15:45097923..45101534hg38UCSC Ensembl
Outerchr15:45097900..45101557hg38UCSC Ensembl
chr15:45390109..45393743hg19UCSC Ensembl
Innerchr15:45390121..45393732hg19UCSC Ensembl
Outerchr15:45390098..45393755hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg383635
hg193635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233729
SamplesHG01631
Known GenesDUOX2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636333
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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