A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893029



Internal ID19183849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52369682..52566597hg38UCSC Ensembl
Outerchr17:52369682..52566597hg38UCSC Ensembl
Innerchr17:50447042..50643957hg19UCSC Ensembl
Outerchr17:50447042..50643957hg19UCSC Ensembl
Innerchr17:47802041..47998956hg18UCSC Ensembl
Outerchr17:47802041..47998956hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38196916
hg19196916
hg18196916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781031
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893029
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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