A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891623



Internal ID19186019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16783382..16904848hg38UCSC Ensembl
Outerchr9:16783382..16904848hg38UCSC Ensembl
Innerchr9:16783380..16904846hg19UCSC Ensembl
Outerchr9:16783380..16904846hg19UCSC Ensembl
Innerchr9:16773380..16894846hg18UCSC Ensembl
Outerchr9:16773380..16894846hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38121467
hg19121467
hg18121467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790538, essv25790334
Samples
Known GenesBNC2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891623
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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