A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614299



Internal ID16401708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60947555..60968775hg38UCSC Ensembl
Innerchr9:39918046..39939299hg19UCSC Ensembl
Innerchr9:39908046..39929299hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3821221
hg1921254
hg1821254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134112, nssv1134111, nssv1134110, nssv1134113
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614299
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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