A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636772



Internal ID6676879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66704212..66712175hg38UCSC Ensembl
Innerchr15:66704243..66712144hg38UCSC Ensembl
Outerchr15:66704181..66712206hg38UCSC Ensembl
chr15:66996550..67004513hg19UCSC Ensembl
Innerchr15:66996581..67004482hg19UCSC Ensembl
Outerchr15:66996519..67004544hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg387964
hg197964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15274262, essv15274263
SamplesHG00306, HG02699
Known GenesSMAD6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636772
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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