A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549045



Internal ID15989768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:205909560..205915146hg38UCSC Ensembl
Innerchr1:205878688..205884274hg19UCSC Ensembl
Innerchr1:204145311..204150897hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg385587
hg195587
hg185587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv734944
Samples
Known GenesSLC26A9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549045
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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