A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891629



Internal ID18839339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17496116..17537072hg38UCSC Ensembl
Outerchr9:17493939..17539322hg38UCSC Ensembl
Innerchr9:17496114..17537070hg19UCSC Ensembl
Outerchr9:17493937..17539320hg19UCSC Ensembl
Innerchr9:17486114..17527070hg18UCSC Ensembl
Outerchr9:17483937..17529320hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3845384
hg1945384
hg1845384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796588, essv25796173, essv25796230, essv25779422
Samples
Known GenesCNTLN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891629
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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