A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789100



Internal ID18823996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12794693..12854043hg38UCSC Ensembl
Innerchr1:12854842..12913896hg19UCSC Ensembl
Innerchr1:12777429..12836483hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3859351
hg1959055
hg1859055
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891192
Supporting Variants
Samples
Known GenesHNRNPCL1, LOC649330, PRAMEF1, PRAMEF11
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789100
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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