A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6492784



Internal ID8993915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33470837..33471009hg38UCSC Ensembl
chr17:31797855..31798027hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666858
Supporting Variants
SamplesHG00590
Known GenesASIC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6492784
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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