A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891568



Internal ID19185964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10723877..10770620hg38UCSC Ensembl
Outerchr9:10723877..10770620hg38UCSC Ensembl
Innerchr9:10723877..10770620hg19UCSC Ensembl
Outerchr9:10723877..10770620hg19UCSC Ensembl
Innerchr9:10713877..10760620hg18UCSC Ensembl
Outerchr9:10713877..10760620hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3846744
hg1946744
hg1846744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786071
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891568
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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