A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664534



Internal ID9930639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79902094..79902434hg38UCSC Ensembl
Outerchr17:79902057..79902484hg38UCSC Ensembl
Innerchr17:77875893..77876233hg19UCSC Ensembl
Outerchr17:77875856..77876283hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6536518, essv5578167
SamplesHG01101, HG01489
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664534
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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