A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780744



Internal ID18820063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90335679..90681223hg38UCSC Ensembl
Innerchr7:89964993..90310537hg19UCSC Ensembl
Innerchr7:89802929..90148473hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38345545
hg19345545
hg18345545
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891163
Supporting Variants
Samples
Known GenesCDK14, CLDN12, GTPBP10, LOC101409256
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=98
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780744
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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