A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640306



Internal ID7027081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28250904..28263402hg38UCSC Ensembl
Innerchr17:28250910..28263396hg38UCSC Ensembl
Outerchr17:28250898..28263408hg38UCSC Ensembl
chr17:26577930..26590428hg19UCSC Ensembl
Innerchr17:26577936..26590422hg19UCSC Ensembl
Outerchr17:26577924..26590434hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3812499
hg1912499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15655837
SamplesNA12282
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640306
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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