A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1146681



Internal ID15999867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134060329..134125912hg38UCSC Ensembl
Innerchr9:136925451..136991034hg19UCSC Ensembl
Innerchr9:135915272..135980855hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3865584
hg1965584
hg1865584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615780
Supporting Variants
Samples
Known GenesBRD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1146681
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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