A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640861



Internal ID7027635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56953281..56954470hg38UCSC Ensembl
Innerchr17:56953331..56954389hg38UCSC Ensembl
Outerchr17:56953208..56954543hg38UCSC Ensembl
chr17:55030642..55031831hg19UCSC Ensembl
Innerchr17:55030692..55031750hg19UCSC Ensembl
Outerchr17:55030569..55031904hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15707030, essv15707031
SamplesHG03378, HG03548
Known GenesCOIL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640861
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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