A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797771



Internal ID18817206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104391828..106660921hg38UCSC Ensembl
Innerchr9:107154109..109423202hg19UCSC Ensembl
Innerchr9:106193930..108463023hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382269094
hg192269094
hg182269094
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891705
Supporting Variants
Samples
Known GenesABCA1, FKTN, FSD1L, LOC100996590, LOC286367, MIR8081, NIPSNAP3A, NIPSNAP3B, OR13C2, OR13C3, OR13C4, OR13C5, OR13C8, OR13C9, OR13D1, OR13F1, SLC44A1, TAL2, TMEM38B
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=579
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797771
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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