A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891627



Internal ID18839337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17096755..17219244hg38UCSC Ensembl
Outerchr9:17096755..17219244hg38UCSC Ensembl
Innerchr9:17096753..17219242hg19UCSC Ensembl
Outerchr9:17096753..17219242hg19UCSC Ensembl
Innerchr9:17086753..17209242hg18UCSC Ensembl
Outerchr9:17086753..17209242hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38122490
hg19122490
hg18122490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786785
Samples
Known GenesCNTLN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891627
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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