A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615946



Internal ID16403355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136059167..136133769hg38UCSC Ensembl
Innerchr9:138951013..139025615hg19UCSC Ensembl
Innerchr9:138090834..138165436hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3874603
hg1974603
hg1874603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148287
Samples
Known GenesC9orf69, NACC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615946
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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