A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784922



Internal ID19173379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19059330..19181489hg38UCSC Ensembl
Innerchr17:18962643..19084802hg19UCSC Ensembl
Innerchr17:18903368..19025395hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38122160
hg19122160
hg18122028
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892975
Supporting Variants
Samples
Known GenesGRAPL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784922
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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