A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636903



Internal ID6677010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74336145..74342188hg38UCSC Ensembl
Innerchr15:74336154..74342180hg38UCSC Ensembl
Outerchr15:74336137..74342197hg38UCSC Ensembl
chr15:74628486..74634529hg19UCSC Ensembl
Innerchr15:74628495..74634521hg19UCSC Ensembl
Outerchr15:74628478..74634538hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg386044
hg196044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15292811
SamplesHG01973
Known GenesCYP11A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636903
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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