A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791877



Internal ID18825639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57788604..58390307hg38UCSC Ensembl
Innerchr6:58031024..58716585hg19UCSC Ensembl
Innerchr6:58138983..58824544hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg38601704
hg19685562
hg18685562
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890851
Supporting Variants
Samples
Known GenesGUSBP4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=78
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791877
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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