A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6234298



Internal ID9211701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74886450..74890181hg38UCSC Ensembl
chr17:72882582..72886306hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg383732
hg193725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670185
Supporting Variants
SamplesHG00693
Known GenesFADS6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6234298
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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