A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787804



Internal ID19170495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:105394590..105530029hg38UCSC Ensembl
Innerchr7:105035037..105170476hg19UCSC Ensembl
Innerchr7:104822273..104957712hg18UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg38135440
hg19135440
hg18135440
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891174
Supporting Variants
Samples
Known GenesPUS7
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787804
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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