A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786785



Internal ID18834248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17096755..17219244hg38UCSC Ensembl
Innerchr9:17096753..17219242hg19UCSC Ensembl
Innerchr9:17086753..17209242hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38122490
hg19122490
hg18122490
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891627
Supporting Variants
Samples
Known GenesCNTLN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786785
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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