A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891700



Internal ID19186096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103096195..103364587hg38UCSC Ensembl
Outerchr9:103096195..103364587hg38UCSC Ensembl
Innerchr9:105858477..106126869hg19UCSC Ensembl
Outerchr9:105858477..106126869hg19UCSC Ensembl
Innerchr9:104898298..105166690hg18UCSC Ensembl
Outerchr9:104898298..105166690hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38268393
hg19268393
hg18268393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789244
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891700
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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