A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615343



Internal ID16056066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127407595..127423429hg38UCSC Ensembl
Innerchr9:130169874..130185708hg19UCSC Ensembl
Innerchr9:129209695..129225529hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3815835
hg1915835
hg1815835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141451
Samples
Known GenesSLC2A8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615343
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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