A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659199



Internal ID9925304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4902253..4907056hg38UCSC Ensembl
Outerchr16:4902192..4907114hg38UCSC Ensembl
Innerchr16:4952254..4957057hg19UCSC Ensembl
Outerchr16:4952193..4957115hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384923
hg194923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6311603
SamplesHG00592
Known GenesPPL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659199
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