A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891528



Internal ID19185924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4255088..4321558hg38UCSC Ensembl
Outerchr9:4255088..4321558hg38UCSC Ensembl
Innerchr9:4255088..4321558hg19UCSC Ensembl
Outerchr9:4255088..4321558hg19UCSC Ensembl
Innerchr9:4245088..4311558hg18UCSC Ensembl
Outerchr9:4245088..4311558hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3866471
hg1966471
hg1866471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789657
Samples
Known GenesGLIS3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891528
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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