A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788512



Internal ID18817252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:60392..223067hg38UCSC Ensembl
Innerchr7:60392..223067hg19UCSC Ensembl
Innerchr7:155475..318150hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38162676
hg19162676
hg18162676
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891006
Supporting Variants
Samples
Known GenesFAM20C, LOC100507642
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=41
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788512
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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