A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663202



Internal ID9929307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63848822..63849727hg38UCSC Ensembl
Outerchr17:63848665..63849880hg38UCSC Ensembl
Innerchr17:61926182..61927087hg19UCSC Ensembl
Outerchr17:61926025..61927240hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg381216
hg191216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5644919, essv6016036
SamplesHG00705, HG00620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663202
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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