A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792689



Internal ID19173611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144038464..144135334hg38UCSC Ensembl
Innerchr4:144959617..145056487hg19UCSC Ensembl
Innerchr4:145179067..145275937hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3896871
hg1996871
hg1896871
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894043
Supporting Variants
Samples
Known GenesGYPA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792689
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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