A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659969



Internal ID9926074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34239107..34242943hg38UCSC Ensembl
Outerchr15:34239070..34242993hg38UCSC Ensembl
Innerchr15:34531308..34535144hg19UCSC Ensembl
Outerchr15:34531271..34535194hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383924
hg193924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6159168
SamplesNA19700
Known GenesSLC12A6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659969
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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