A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797686



Internal ID19181326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148175413..148186515hg38UCSC Ensembl
Innerchr7:147872505..147883607hg19UCSC Ensembl
Innerchr7:147503438..147514540hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3811103
hg1911103
hg1811103
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891231
Supporting Variants
Samples
Known GenesCNTNAP2, MIR548T
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797686
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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