A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792840



Internal ID19175624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22170862..22756949hg38UCSC Ensembl
Innerchr17:21697468..22256276hg19UCSC Ensembl
Innerchr17:21621598..22180403hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg38586088
hg19558809
hg18558806
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892985
Supporting Variants
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=89
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792840
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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