A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779317



Internal ID18822423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161521106..161654964hg38UCSC Ensembl
Innerchr1:161490896..161624754hg19UCSC Ensembl
Innerchr1:159757520..159891378hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38133859
hg19133859
hg18133859
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890693
Supporting Variants
Samples
Known GenesFCGR2C, FCGR3A, FCGR3B, HSPA6, HSPA7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779317
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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