A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25793012



Internal ID19170069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22701708..22756949hg38UCSC Ensembl
Innerchr17:22201035..22256276hg19UCSC Ensembl
Innerchr17:22125162..22180403hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg3855242
hg1955242
hg1855242
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892987
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25793012
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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