A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891664



Internal ID19186060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60936108..61000253hg38UCSC Ensembl
Outerchr9:60936108..61000253hg38UCSC Ensembl
Innerchr9:39906602..39970742hg19UCSC Ensembl
Outerchr9:39906602..39970742hg19UCSC Ensembl
Innerchr9:39896602..39960742hg18UCSC Ensembl
Outerchr9:39896602..39960742hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3864146
hg1964141
hg1864141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786395
Samples
Known GenesFAM74A1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891664
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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