A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891638



Internal ID19186034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22913605..22999427hg38UCSC Ensembl
Outerchr9:22913605..22999427hg38UCSC Ensembl
Innerchr9:22913604..22999426hg19UCSC Ensembl
Outerchr9:22913604..22999426hg19UCSC Ensembl
Innerchr9:22903604..22989426hg18UCSC Ensembl
Outerchr9:22903604..22989426hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3885823
hg1985823
hg1885823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799629
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891638
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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