A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892985



Internal ID19183805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22170862..22756949hg38UCSC Ensembl
Outerchr17:22170862..22756949hg38UCSC Ensembl
Innerchr17:21697468..22256276hg19UCSC Ensembl
Outerchr17:21697468..22256276hg19UCSC Ensembl
Innerchr17:21621598..22180403hg18UCSC Ensembl
Outerchr17:21621598..22180403hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg38586088
hg19558809
hg18558806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792840
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892985
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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