A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796173



Internal ID18817531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17493939..17539322hg38UCSC Ensembl
Innerchr9:17493937..17539320hg19UCSC Ensembl
Innerchr9:17483937..17529320hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3845384
hg1945384
hg1845384
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891629
Supporting Variants
Samples
Known GenesCNTLN
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796173
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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