A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782988



Internal ID19164002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54758465..54775562hg38UCSC Ensembl
Innerchr17:52835826..52852923hg19UCSC Ensembl
Innerchr17:50190825..50207922hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3817098
hg1917098
hg1817098
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893032
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782988
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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