A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640311



Internal ID6680398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28519801..28523624hg38UCSC Ensembl
Innerchr17:28519801..28523624hg38UCSC Ensembl
Outerchr17:28519664..28523854hg38UCSC Ensembl
chr17:26846819..26850642hg19UCSC Ensembl
Innerchr17:26846819..26850642hg19UCSC Ensembl
Outerchr17:26846682..26850872hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383824
hg193824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15656915
SamplesNA12347
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640311
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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