A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6316265



Internal ID9293668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42714765..42714878hg38UCSC Ensembl
Outerchr21:42714728..42714928hg38UCSC Ensembl
Innerchr21:44134875..44134988hg19UCSC Ensembl
Outerchr21:44134838..44135038hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675114
Supporting Variants
SamplesNA18557
Known GenesPDE9A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6316265
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