A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615212



Internal ID16055935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113128729..113153579hg38UCSC Ensembl
Innerchr9:115891009..115915859hg19UCSC Ensembl
Innerchr9:114930830..114955680hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3824851
hg1924851
hg1824851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141256
Samples
Known GenesSLC31A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615212
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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