A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6363930



Internal ID9341333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68552650..68552980hg38UCSC Ensembl
chr17:66548791..66549121hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677068
Supporting Variants
SamplesNA20539
Known GenesFAM20A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6363930
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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