A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5612277



Internal ID9407866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11667663..11668535hg38UCSC Ensembl
chr17:11570980..11571852hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663712
Supporting Variants
SamplesNA18611
Known GenesDNAH9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5612277
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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