A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891163



Internal ID18838873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90335679..90681223hg38UCSC Ensembl
Outerchr7:90335679..90681223hg38UCSC Ensembl
Innerchr7:89964993..90310537hg19UCSC Ensembl
Outerchr7:89964993..90310537hg19UCSC Ensembl
Innerchr7:89802929..90148473hg18UCSC Ensembl
Outerchr7:89802929..90148473hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38345545
hg19345545
hg18345545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780744
Samples
Known GenesCDK14, CLDN12, GTPBP10, LOC101409256
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891163
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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