A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786694



Internal ID19163093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19021812..19181371hg38UCSC Ensembl
Innerchr17:18925125..19084684hg19UCSC Ensembl
Innerchr17:18865850..19025277hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38159560
hg19159560
hg18159428
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892975
Supporting Variants
Samples
Known GenesGRAP, GRAPL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786694
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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