A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640873



Internal ID7027647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57507584..57512140hg38UCSC Ensembl
Innerchr17:57507632..57512093hg38UCSC Ensembl
Outerchr17:57507537..57512188hg38UCSC Ensembl
chr17:55584945..55589501hg19UCSC Ensembl
Innerchr17:55584993..55589454hg19UCSC Ensembl
Outerchr17:55584898..55589549hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384557
hg194557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15708185
SamplesNA20854
Known GenesMSI2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640873
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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