A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781031



Internal ID19162759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52369682..52566597hg38UCSC Ensembl
Innerchr17:50447042..50643957hg19UCSC Ensembl
Innerchr17:47802041..47998956hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38196916
hg19196916
hg18196916
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893029
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781031
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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