A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664082



Internal ID9930187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75319745..75350706hg38UCSC Ensembl
Outerchr16:75319708..75350756hg38UCSC Ensembl
Innerchr16:75353643..75384604hg19UCSC Ensembl
Outerchr16:75353606..75384654hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3831049
hg1931049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5874633
SamplesNA19901
Known GenesCFDP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664082
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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