A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890693



Internal ID19184995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161523790..161654964hg38UCSC Ensembl
Outerchr1:161521106..161654964hg38UCSC Ensembl
Innerchr1:161493580..161624754hg19UCSC Ensembl
Outerchr1:161490896..161624754hg19UCSC Ensembl
Innerchr1:159760204..159891378hg18UCSC Ensembl
Outerchr1:159757520..159891378hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38133859
hg19133859
hg18133859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801433, essv25779317
Samples
Known GenesFCGR2C, FCGR3A, FCGR3B, HSPA6, HSPA7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890693
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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