A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783588



Internal ID19160578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19014011..19180622hg38UCSC Ensembl
Innerchr17:18917324..19083935hg19UCSC Ensembl
Innerchr17:18858049..19024528hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38166612
hg19166612
hg18166480
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892975
Supporting Variants
Samples
Known GenesGRAP, GRAPL, SLC5A10
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783588
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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