A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891652



Internal ID18839362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29906486..31116345hg38UCSC Ensembl
Outerchr9:29906486..31116345hg38UCSC Ensembl
Innerchr9:29906484..31116343hg19UCSC Ensembl
Outerchr9:29906484..31116343hg19UCSC Ensembl
Innerchr9:29896484..31106343hg18UCSC Ensembl
Outerchr9:29896484..31106343hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381209860
hg191209860
hg181209860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791921
Samples
Known GenesLOC401497
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891652
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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