A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891502



Internal ID19185898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:398673..629437hg38UCSC Ensembl
Outerchr9:297394..686301hg38UCSC Ensembl
Innerchr9:398673..629437hg19UCSC Ensembl
Outerchr9:297394..686301hg19UCSC Ensembl
Innerchr9:388673..619437hg18UCSC Ensembl
Outerchr9:287394..676301hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38388908
hg19388908
hg18388908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788841, essv25788672, essv25788519, essv25788229
Samples
Known GenesDOCK8, KANK1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891502
Frequency
Sample Size3017
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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