A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640130



Internal ID7026907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17605123..17611823hg38UCSC Ensembl
Innerchr17:17605150..17611796hg38UCSC Ensembl
Outerchr17:17605096..17611850hg38UCSC Ensembl
chr17:17508437..17515137hg19UCSC Ensembl
Innerchr17:17508464..17515110hg19UCSC Ensembl
Outerchr17:17508410..17515164hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg386701
hg196701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15635774
SamplesNA19066
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640130
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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