A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15274263



Internal ID5276079
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636772
Supporting Variants
SamplesHG02699
Known GenesSMAD6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15274263
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer