A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779862



Internal ID19165030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19003716..19181489hg38UCSC Ensembl
Innerchr17:18907029..19084802hg19UCSC Ensembl
Innerchr17:18847754..19025395hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38177774
hg19177774
hg18177642
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892975
Supporting Variants
Samples
Known GenesFAM83G, GRAP, GRAPL, SLC5A10
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779862
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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