A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640898



Internal ID7027672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58922185..58937823hg38UCSC Ensembl
Innerchr17:58922685..58937323hg38UCSC Ensembl
Outerchr17:58921185..58938823hg38UCSC Ensembl
chr17:56999546..57015184hg19UCSC Ensembl
Innerchr17:57000046..57014684hg19UCSC Ensembl
Outerchr17:56998546..57016184hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3815639
hg1915639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15711246, essv15711247, essv15711245
SamplesHG03086, NA18516, NA19438
Known GenesPPM1E
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640898
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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