A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891678



Internal ID18839388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68918451..69072734hg38UCSC Ensembl
Outerchr9:68918451..69144626hg38UCSC Ensembl
Innerchr9:71533367..71687650hg19UCSC Ensembl
Outerchr9:71533367..71759542hg19UCSC Ensembl
Innerchr9:70723187..70877470hg18UCSC Ensembl
Outerchr9:70723187..70949362hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38226176
hg19226176
hg18226176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788959, essv25788860, essv25788993, essv25788842
Samples
Known GenesFXN, PIP5K1B, PRKACG, TJP2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891678
Frequency
Sample Size3017
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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