A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615571



Internal ID16056294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132118176..132180427hg38UCSC Ensembl
Innerchr9:134993563..135055814hg19UCSC Ensembl
Innerchr9:133983384..134045635hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3862252
hg1962252
hg1862252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1145325
Samples
Known GenesNTNG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615571
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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